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RyMed's patented disruptive technology provides the only clinically -
proven solution in combating both Catheter -related Bloodstream Infections
(CR-BSIs) and Intraluminal Thrombotic Catheter Occlusions (Blood Clots),
two of the most severe patient issues plaguing Healthcare today.
Investor Presentation
February 2012
1 Middlebury
Group
EFTA01117402
Safe Harbor Statement
All statements other than statements of historical facts included herein regarding the Company's
financial position, business strategy, growth strategy and other plans and objectives for future
operations, are forward -looking statements. The words "anticipate," "believe," "estimate,"
"expect," "intend," "plan" and similar expressions that may tend to suggest a future event or
outcome are not guarantees of performance and are inherently subject to numerous risks and
uncertainties, many of which cannot be predicted or anticipated. Future events and actual
results, financial or otherwise, could differ materially from those contained herein. Potential
investors are cautioned that any such forward -looking statements are not guarantees of future
performance and involve significant risks and uncertainties, and that actual results may differ
materially from those projected in the forward -looking statements as a result of various factors.
Potential investors are urged to carefully consider all risk-factors highlighted in the private
placement memorandum. All forward -looking statements are expressly qualified in their entirety
by the foregoing cautionary statement. This is not a solicitation to sell nor offer to buy.
RyMed Technologies, Inc.
137 Third Avenue North
Franklin, TN 37064
www.rymedtech.com
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TECHNOLOGIES, INC.
EFTA01117403
Creation of a Problem
Prior to RyMed's InVision-Plus® technology introduction in May 2004, Needleless
I.V. Connector Systems were designed to protect healthcare professionals from
accidental needle stick injuries, AIDS and hepatitis transmission.
Unbeknown to the design engineers, they solved one problem by protecting the
healthcare worker from accidental needle stick injuries, BUT created a new patient
safety problem.
Vascular Access Healthcare Crisis
• 250,000 — 500,000 catheter-related bloodstream infections yearly in US *
• 12-25% mortality rate associated with an intravascular-related BSI*
• ICU Length of Stay can increase by as much as 20 days; hospitals by 22 days*
❖ $2.3 - S28 Billion/year spent to treat CR-BSIs*
'Maki. D. G.. Kluge, D M . & Crnich. C J (2006). May Clinic Proceedings. 81(9). 1159-1171.
Needleless I.V. Connector Product Design Flaws
All competitive (Negative & Positive) needleless I.V. connector designs exhibit one or more fluid
pathway concerns:
Negative Fluid Displacement Lack of Septum Seal Integrity
Fluid Pathway Dead Space Ineffective Septum Surface Design
Tortuous Fluid Pathways
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- TECHNOLOGIES, INC. 3
EFTA01117404
Neutral Advantage" technology RyMed's "10-Point Standard"
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TECHNOLOGIES INC RyMed's patented InVision-Plus® Needleless I.V. Connector System is
believed to be the first and only product of its kind that was created from the
"ground up" in order to protect patients from the two critical vascular access
catheter issues facing healthcare worldwide
EFTA01117405
The Advantage is Clear Statement
Negative Fluid Displacement
Baxter ClearLink®(example) RyMed Technologies
The ONLY Zero Fluid Displacement System
Negative fluid displacement, or blood refluxing into the catheter lumen, develops
blood fibrin, a food source for micro-organisms that develops into biofilm
colonization, a source of catheter bloodstream infections.
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EFTA01117406
Snapshot RyMed
HISTORY: 1994 Company Founded
1997 InVision-Plus® Development Began
2004 Market Introduction
2006 Began hiring Direct Sales Force
2007 InVision-Plus® Red® Introduction
2008 InVision-Plus® Junior® Introduction
2009 InVision-Plus® Epi® Introduction
2010 Walgreens National Formulary (April)
FDA Alert — Positive Pressure IV connectors
FDA Clearance — In Vision-Plus® CS TM
2011 CS® beta site product trials began
CVS Caremark (April)
Amerinet - First GPO Contract
HEADQUARTERS:
OPERATIONS:
MANUFACTURING:
EMPLOYEE COUNT: Franklin, TN
Austin, TX
El Paso, TX/Juarez Mexico
23 Recent *News*
July 2011 iData Research , Vancouver British
Columbia Canada stated RyMed
Technologies is one of the major
forces in Needleless IV Connectors in
the U.S. Market
November US Army began purchasing
December Company received supply
contract from Mayo Clinic's
January 2012 Two supportive peer-reviewed
clinical poster presentations accepted
by Oncology Nursing Society Europe
Geneva — April
January B-D Posi-Flo® and Baxter Flo-Link®
Positive Pressure Needleless IV
Connector discontinued.
Revenue $5,095 56,239 $7,088 $13,084 $22,800
Net Income ($6,070) (53,263) ($2,794) $890 98,851
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EFTA01117407
RyMed Snapshot 2012 Sales Projection
2011 Actual
2012 SALES PLAN
U.S. Field Sales Plan
OEM Sales
InVision-Plus® CS® Sales
International Sales
TOTAL SALES PLAN $ 7.1 MM (To Distributors)
$ 9.5 MM
$ 0.8 MM
$ 2.2 MM
$ 0.6 MM
$ 13.1 MM + 84.2%
2012Sales Force Expansion: Add an additional 13 field sales representatives (April-June 2012)
Add two new clinical RNs (April-June 2012)
New Controller (Feb 2012)
New Senior Director, Marketing & Clinical Education (Feb 2012)
New Director, National Accounts position (Jan 2012)
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EFTA01117408
RyMed Snapshot 2012 U.S. Market Landscape
Clinical Proof of InVision-Plus® Safety & Efficacy - Exceeding Expectations
New InVision-Plus® CS® with Chlorhexidine + Silver Ion Technology
A NEW TRANSFORMATIONAL NEEDLELESS IV CONNECTOR SYSTEM
> Received FDA 510(k) Approval
> Kills the eight (8) common microorganisms associated with CR-BSIs
> Full seven (7) day usage potential
> A 7.0 log reduction of MRSA
> All beta-sites reported "zero" CR-BSIs during their trial period in 2011
Medicare Non-Reimbursement for CR-BSIs
VA Hospitals Alert Warning of Positive Pressure Needless IV Connectors
FDA Alert & Notification of Positive Pressure Needleless IV Connectors
Dr. Jarvis M.D. — Clinical Journal Articles on potential risks for CR-BSIs
Dr. Jarvis M.D. — Clinical Journal Article on competitive "Silver-only"
Needleless IV Connectors - Blood Inactivates (Reported to be published in 2012)
Baxter Healthcare V-Link®
> Care Fusion Max-GuardTm (Positive Pressure)
> B. Braun UltraSite Ag TM (Positive Pressure)
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TECHNOLOGIES, IN
EFTA01117409
RyMed Snapshot 2012 U.S. Market & Sales Landscape
iData Research Study - U.S. Vascular Access Market Needleless IV Connectors will be the driving force within healthcare facilities
RyMed Technologies - One of the major forces in Needleless IV Connectors
Continued standardization trend PICCs, CVCs and PIVs — (1) Needleless IV Connector
• Shorter sales cycle time from introduction
ft- New emphasis from "C-Suite" administrators New attitude on CR-BSIs - "Soft Savings- . "Hard Savings"
Eliminate CR-BSIs - Reduce Costs and Risks
First major GPO — Amerinet (September 2011)
• 2.700+ member hospitals. IDNs
Paul Blackburn — New Senior Director, Marketing & Clinical Education • Starting Date: February 13. 2012
• Coming from Bard-Access Systems
• New President-elect — Association for Vascular Access (AVA - Sept 2012)
Jim Hinkel — New Controller Starting Date: February 1. 2012
ICU Medical Litigation • Most Clave and MicroClave U.S. patents expired December 18. 2011:
Improved clarity with new trial - May 7. 2012:
One patent, one independent claim: literal infringement only
RyMed's new "work around" component design
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EFTA01117410
Needleless I.V.. Comactees ", US USW Siam
2011: 1.32 Billion Units x $2.65 = $3.5 Billion
2016: 1.84 Billion Units x $3.50 = $6.5 Billion
CAGR 111 - 16') - +7.1%
Total U.S. UNIT Market Projections - Needleless I.V. Connectors
Fr- 2,250
2,000 1,844
1,750 1,625 1.732
1.521
1,500 1,420
1,321
1,250 1,227
1,000
750
500
250
0
2010 2011 2012 2013 2014 2015 2016 A
M Ad Source: iData Research Inc., Vancouver, Canada U.S. Market
for Vascular Access Devices and Accessories, February 2010
- TECHNOLOGIES, INC. 10
EFTA01117411
Design Evolution Needleless IV Connector Devices
• Recessed needles (late 1980s)
- No negative fluid displacement
• Split Septum or Blunt Cannula devices with Negative Fluid Displacement (early 1990s)
- Negative fluid displacement upon disconnection
— Dr. William Jarvis MD article "Increased CR-BSIs associated with the use of Negative and Positive
Displacement Needleless IV Connectors"
• Luer-Activated devices with Negative Displacement (mid 1990s)
Negative fluid displacement upon disconnection
Dr. William Jarvis MD article "Increased CR-BSIs associated with the use of Negative and Positive
Displacement Needleless IV Connectors"
• Luer-Activated devices with Positive Fluid Displacement (late 1990s)
Negative fluid displacement upon connection
VA Administration Warning Letter — December 2007
FDA Alert & Notification Letter — July 2010
Dr. William Jarvis MD article "Increased CR-BSIs associated with the use of Negative and Positive
Displacement Needleless IV Connectors"
• RyMed's InVision-Plus® (Introduction May 2004)
- Neutral Fluid Displacement (Patent Issued)
- Zero Fluid Displacement (Patent Issued — January 2012)
- Double Microbial Barrier Design (Patented technology)
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EFTA01117412
RyMed's Competitors
Clinical Infectious Diseases 2009: 49-1821-7
"Health care-associated, central venous catheter-related
bloodstream infections (HA-BSIs) are a major cause of
morbidity and mortality"
"Needleless connectors are an important component of
the intravenous system"
"Needleless connectors initially were introduced to reduce
health care worker needle stick injuries, yet some of
these needleless connectors may increase HA-BSI risk"
"The Centers for Disease Control and Prevention (CDC)
estimates that, in US intensive care unit (ICU) patients,
> 80,000 HA-BSIs occur, costing up to $29 billion
annually."
Conclusions: "We found strong evidence that Mechanical
Valve Needleless Connectors (MV-NCs) were associated
with increased HA-BSI rates, despite similar BSI
surveillance, definitions, and prevention strategies" MAJOR ARUM
Health Care—Associated Bloodsucam Infections
Associated with Negative- or Positive-Prev,on:
or Displacement NtetiLmical \IdNe NeedleleNs
Connectors
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EFTA01117413
Federal Medicare Mandates
October 2008
Medicare stopped paying hospitals for treating the following conditions:
Catheter -associated urinary tract infections
Pressure ulcers
• Vascular catheter-associated infections (CR-BSIs)
• Mediastinitis after coronary artery bypass
• Fractures, dislocations, or other injuries
• Objects left in during surgery
• Air embolisms
• Blood incompatibilities
July 2010
FDA notifies Infection Control Officer's and Manufacturers via the ALERT &
NOTIFICATION LETTER on Positive Displacement I.V. Connectors
RifMed is believed to be the ONLY MANUFACTURER selling
in the U.S. not cited in this FDA Alert
13
EFTA01117414
Product Technology
EFTA01117415
Segmentation Strategy
The S • ectrum of Protection® Line of Products
CM:
IRtnewoolnal Prot.-al.. System
Iesifon-Plas
iziViii;;;iiiiii ,, Designed for all I.V. and Blood Administration/Blood Sampling
Designed for Visual Identification of Non-Venous Catheters
Designed for Neonatal & Pediatric Patients
Designed for use with Pain Management Catheters
RyMed/Bacterin International Chlorhexidine+Silver Ion
A new transformational technoloav
gill V it'll INC 15
EFTA01117416
A new transformational technology
RyMed Technologies new anti-bacterial InVision-Plus® CS® with Chlorhexidine + Silver Ions within its
patented "Double Microbial Barrier" design does not come in contact with the patients blood. It is
the first and only Needleless I.V. Connector System in the world that has received FDA or other
regulatory body approval clearance with Cag and up to 7 days of usage.
Kills the 8 common microorganisms associated with CR-BSIs
Up to a 7.0 Log (99.99999%) Reduction MRSA — 7 days
RyMed's Competition:
In a recent in-vitro study by Nelson Laboratories, Salt Lake City, UT on the "silver only" anti-bacterial I.V.
connectors, it was discovered that competitive products shield the silver from the micro-organisms with a coating
of blood fibrin. Each of the competitive connectors actually grew micro-organisms as reported in the study.
Baxter Healthcare V-Link®
•Silver only coated fluid pathway
•96 hour effectiveness
•Negative Fluid Displacement B. Braun UltraSite Ag®
. Silver only impregnated fluid pathway components
. 96 hour effectiveness
. Positive Pressure Displacement (FDA Alert)
CareFusion MaxGuard®
. Silver only impregnated fluid pathway components
. 24 hour effectiveness
. Positive Pressure Displacement (FDA Alert)
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TECHNOLOGIES, INC 16
EFTA01117417
Beta Site Trills I nVision-Plus® CS® with Chlorhexidine + Silver Ions
2011
4 Beta Site Product Trials
Phoenix Children's (PICU), Phoenix, AZ
. 90 day trial — All patients, all lines
. Product trial completed — Reported "Zero" CR-BSIs
Los Angeles Medical Center (NICU) — Kaiser Permanente
. 90 day trial - Neonatal patients
. Product trial completed — Reported "Zero" CR-BSIs
Methodist Long-Term Care Hospital, Memphis, TN
. 90 day trial — All patients, all lines
. Product trial completed — Reported "Zero" CR-BSIs
Duke University Medical Center, Durham, NC
. 120 day trial — All patients, all lines — Oncology Department
. Product trial completed — Reported "Zero" CR-BSIs
ACTION PLAN: HIGH VOLUME SCALE-UP PROCESS IS BEING FINALIZED
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TECHNOLOGIES, INC 17
EFTA01117418
Intellectual Property
• Nine (9) U.S. Patents Issued
Five U.S. Patents Issued on InVision-Plus technology)
InVision-Plus current IP runs from 2023 through 2032
- Double Microbial Barrier
- 3 Piece Valve System
- Neutral Fluid Displacement
- Zero Fluid Displacement
• Foreign Patents Issued
- All major markets
- Additional pending
• Numerous Trademarks Registered & Pending
EFTA01117419
Positive Patient Results
rialinderson_C.ancet.Cente
(Monthly Average Occlusion Incidence)
Split-Septum:
InVision-Plus®:
Reduction %: ICU
15.3
12.3
20% t - • s .
In-Patient
8.3
4.5
■ 46%
Sutter Hospital Roseville. CA
200 Bed Community Hospital
Before InVision-Plus® Implementation
2005 - 767 11 CR-BSI
I or caring for 1 CR-BSI - $25,000 - $56,000
,A [ter InVision-Plus*
2006 —1,558
2007 — 2,278
2008 - 2,313
2009 > 2,400
2010 > 2,400
2011 > 2,400 0 CR-BSI
0 CR-BSI
0 CR-BSI
0 CR-BSI
0 CR-BSI
0 CR-BSI
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ut-Patient
4.7
0.8
84% RyMed InVision-Plus®
Reduced MD Anderson Cancer Center
catheter infections by 10-fold within
Intensive Care Unit
Texas Children's Hospital
Neonatal Intensive Care Department
The largest NICU department in the U.S.
A total of 288 NICU beds
Before InVision-Plus® is implemented
Monthly CR-BSI Rate -28
After InVision-Plus® is implemented
Monthly CR-BSI Rate - 1 (96% Reduction)
TECNNLLOG/ES, INC 19
EFTA01117420
122,000 Catheter Days of Aggregated Data
Participants in the study reported 178 infections were prevented
and approximately $6.2 million in savings to the hospitals
2011 Association for Professional in Infection Control &
Epidemiology Conference (APIC)
Clinical Comparisons of Split Septum
Positive and Negative Mechanical Valve Intravenous Connectors
to an Intraluminal Protection Connector on Infection Rates
Denim Macklin, BSN, RN-C, Consultant, Marietta, GA Cynthia Chamecky PhD, RN, AOCN, FAAN, Georgia Health Sciences University, Augusta, Georgia
William R. Jervis MD, Jason & Jarvis Associates, LLC, Hilton Head island, SC Jennifer Waller, PhD, Georgia Health Sciences University, Augusta, Georgia
APIC 2011 Baltimore, MD
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Disclosures
EFTA01117421
New Product Development Projects
The Spectrum of Protection® Line of Products
InVision-Plus® HDTM with Chlorhexidine + Silver Ions
for Hemodialysis Catheters
Addressable U.S. Market Size — > 50 Million Units Annually
"Sentry CS(R) Prniect" Anti-Bacterial Prntective End
Caps for Needleless IV Connectors
Addressable U.S. Market Size — > 3.0 Billion Units Annually
"Germinator Project" Cleaning/Disinfection System
Designed to be used on Needleless I.V. Connectors/Catheter Lumens
Addressable U.S. Market Size — > 3.0 Billion Units Annually
Anti-Bacterial Dead End Caps for IV Administration Line
Designed to be used on I.V. Administration Lines
Addressable U.S. Market Size — > 1.0 Billion Units Annually
"Sentry CS Project" Anti-Bacterial Protective End Caps for
Hemodialysis Catheters
IV Start Packs for Peripheral IV Catheter Placement
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EFTA01117422
Distribution Venues
Amerinet
One of six major healthcare "super group" GPO's
Privately owned by Intermountain Healthcare and Administrative Resources, Inc.
Headquartered in Saint Louis, formed in 1986 from smaller regional GPO's
Membership spans the full spectrum of healthcare provider facilities
Membershi
Acute Care Hospitals
Clinics 18
Long-Term Alternate Care Hospitals
Physicians (Hospital Based) 2,
Surgery Centers 2,38
Emergency Medical Services 441
Other 18.347
TOTALS: 51,372
Marquis Alternate Site Accounts
PharMerica National Account
Walgreens National Formulary
CVS Caremark Trials Began
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TECHNOLOGIES, INC,
EFTA01117423
Manufacturing & Operations
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Jim Kaiser
Chief Operations Officer
Operations Office: Austin, TX
23
EFTA01117424
Corporate & Mfg./ Distribution Locations
Z till Z - `•1 • -JO *tr. .4, 5, ON YAM ••
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••• VI * RyMed Headquarters
*Franklin, TN - RyMed
• Distribution Locations:
* Austin. TX - RyMed
* El Paso, TX - Accellent
Sterilization Locations:
* El Paso, TX - STERN
* Santa Teresa, NM - Stcrigenics
* Manufacturing/Assembly Locations:
* Anaheim. CA - HiTech Rubber
* Upland, CA - Accellent
* Juarez, Chihuahua - Accellent
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TECHNOLOGIES, INC
EFTA01117425
Manufacturing and Operations
RyMed Agreements:
Accellent
- Supply and Manufacturing of all products
- Distribution of Finished Goods
- Multi -Year Agreements
- Cancellation with 180 days notice without cause
Benefits: - 60 day payment terms
- Reduced infrastructure
• Materials Planning
• Vendor Audits
• Warehousing Space and Operations
• Payables (virtually one vendor)
- Inventory Reduction Cost Savings
• Inventory Valuation 12-31-2010: $900,113
• Inventory Valuation 12-31-2011: $593,483
Bacterin International
- Treatment of InVision-Plus® Septum component with Chlorhexidine + Silver Ions
- Worldwide, Exclusive Rights for Needle-Free IV Connectors
- Multi -Year with Automatic Renewal
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'I' TECHNOLOGIES, INC 25
EFTA01117426
Current Manufacturing Capacity
RyMed owns a total of 4 assembly machines
• Each Semi-automated module consists of
- Two assembly machines ► Cost: < $ 200,000
- One set of production molds ► Cost: < $ 700,000
• Current annual capacity: 30 million units
- N.A.S.P. - $ 1.58 each (2011)
- Total Sales from current capacity: $ 47.4 million
• Current overall Gross Margin is 53%
- Gross Margin can be improved through:
■ Larger cavitation molds
■ Semi or full automation
- 2012 Target Gross Profit: 60% - 65% with semi-automation
■ > 70% with full automation
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TECHNOLOGIES, INC 26
EFTA01117427
Leadership Financials
Growth Strategy
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EFTA01117428
Management Tam
Dana Wm. Ryan, President & CEO (Founded 1994)
Over 39 years of high volume, disposable medical device experience in sales, management, product marketing,
development. Holds over 35 patents to date worldwide. 3M — sales engineer. Arbrook/Surkigos (J&J) — Head of New
Products Department. Deseret Company ( Warner-Lambert) — Director of Marketing. Ryan Medical — Founder/CEO — 14
patents in safety medical products in the field of blood collection and intravenous therapy. Small Business of the Year
Award, Nashville, TN 1990, Company was sold in 1992. Symbiosis Corporation — Design, develop and manage. Symbiosis
was sold to American Home Products in 1994. Major in mathematics (Arkansas State University). 1968-70 played
professional baseball for the Chicago White Sox organization.
James M. Kaiser, Chief Operations Officer and Financial Director (1997)
Over 40 years of high volume, disposable medical device manufacturing. Cutter Laboratories — manufacturing, sterilization,
and materials management. Deseret Company — Production Superintendent (1,200 employees). Healthcare Group — Vice
President of Operations. Ryan Medical — EVP Manufacturing. Isomedix, inc. — General Manager and later Group VP at HDQ.
MBA (Southland University).
Tony Ryherd, Director of Engineering & Manufacturing (2007)
Over 24 years of industrial manufacturing experience ranging from aerospace engineering to medical device development
and expert in Operation Management Systems. Boeing Aerospace — Lead on China technology transfer. Accellent
Endoscopy — head of engineering development. BS in Manufacturing Engineering (Bradley University).
Brandon D. Ryan, National Sales Director (2006)
Over 12 years leadership experience in medical sales. Began as ABC news anchor, then CBS nightly news anchor/reporter
hosting political roundtable "Behind the Headlines". Bristol-Myers Squibb as Territory Manager. TAP Pharmaceuticals —
Senior Specialty Sales Representative (top performer). BA in Broadcast Journalism (University of Mississippi).
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TECHNOLOGIES, INC 28
EFTA01117429
Management Tea
D. Scott Chase, Director of Marketing (2006)
Over 12 years of composite O.R.based device sales experience,. Techmedica/Sulzer Medica, Inc. (Camarillo, CA), TMJ Implants, Inc.
(Golden, CO), and W. Lorenz Surgical/Biomet, Inc. (Jacksonville, FL), focusing primarily on the sale of titanium and resorbable
craniofacial reconstructive implants, biomaterials and instruments to the neuro, plastic and reconstructive, ENT, oral/maxillofacial
surgical specialties. BA in Mathematics (Vanderbilt University).
Anna McCutchen, Director of Quality Control & Regulatory Affairs (2005)
7 years experience in quality assurance management of government regulated products. Expertise in quality systems, procedures,
documentation and regulations. Triad Foods Group — Quality Assurance Manager. Cargill — Quality Assurance Manager plus plant level
auditing of 7 facilities. BA in Food Science and Technologies (Texas ).
David Rogers, Director of Logistics & Operations Support (2006)
Over 35 years leadership experience in strategic planning, human resources and budgetary controls. In 1967, began career as second
military lieutenant rising to Chief of Staff of the Alaskan Air Command and three times as a Director of Personnel at a Major Air
Command. . Responsible for 3500 person staff with $1.1 billion budget. Numerous military awards and distinctions. Masters Degrees -
University of Arkansas 1974 (Management) and University of Oklahoma 1979 (Public Administration).
Paul L. Blackburn, RN, MNA, Senior Director, Clinical Education (Starting date: February 139')
Over 20 years managerial and clinical education teaching experience. CR-Bard, Bard-Access Systems, Salt Lake City, UT , Director of
Clinical Education. Managed over 150 clinical nurses and team developed all the clinical education programs for Bard-Access PICC
catheter product lines. New President-elect of the Association for Vascular Access (AVA).
Jim Hinkel, Controller (Starting date: February 1st)
Over 30 years of experience in operational accounting, financial analysis, audit responsibility, budgeting, and accounting
control systems.. His experience spans both large and small companies, including a start up company. Jim has a BBA in
Accounting and received his CPA from the State of Illinois (non active).
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I. n s'-. -; TECHNOLOGIES, INC 29
EFTA01117430
Revenue Growth Projection
$25,000,000
$20,000,000
$15,000,000
$10,000,000
$5,000,000
$0 513.054,
$7,087,928
,mingimmummir
2004A 2005A 2006A 2007A 2008A 2009A 2010A 2011A 2012E 2013E
30
EFTA01117431
Summary Financial Statements
Summary Income Statement 2011 Condensed Balance Sheet Dec. 31 2011
ASSETS
Revenue $ 7,081,019 Cash $ 68,500
Cost of Goods Sold 3,337,755 Accounts Receivable 607,756
Gross Profit 3,721,767 Other Current Assets 831,998
Fixed Assets 814,882
SG&A 6,467,986 Other Assets 94.439
Operating Profit/(Loss) (2,746,219) TOTAL $2.417.577
Other (47,895) LIABILITIES
Current $2,021,945
Long Term 4,302,360* Pre-Tax Profit/(Loss) (2,794,114) Total 6,324,305
Taxes -
Net Profit/(Loss) $(2.794.114) . EQUITY ($3,906,729)
TOTAL $2.417,577
TECHNOLOGIES, INC
EFTA01117432
2011 Milestones Lk r• rnmeilichmantc
January
• Began Beta Site Trials with InVision-Plus® CST'' with Chlorhexidine+Silver Ion Engineering
February - March
• 11th National Conference on Cancer Nursing Research — Cynthia Chernecky, PhD
• InVision-Plus® reduced infections and occlusions - Silver treated connectors show ineffectiveness in presence of blood
• Journal of Advanced Nursing — Comparative evaluation of five needleless I.V. connectors; Chernecky & Waller
April - May
• SHEA Conference 2011 — Dallas, TX — Chernecky, Jarvis. Macklin;
• Silver treated needleless connectors show ineffectiveness in presence of blood (abstract poster)
8-states; 122,000 catheter-days; comparative study - InVision-Plus® - Up to 92% reduction in CR-BSIs May
• Naval Hospital, Jacksonville, FL - InVision-Plus product trial
• VA Medical Center, San Antonio, TX — Reported "zero" CRBSIs in product trials
• Spaulding Hospital, Cambridge, MA (Partners) — InVision-Plus product trial*
June
• APIC Conference, Baltimore, MD
. Clinical Poster Presentation —122,000 Catheter Day Study
. Clinical Poster Presentation — Texas Children's Hospital NICU, Houston, TX
• AVA Conference — Accepted Clinical Poster Presentation — Methodist Extended Care Hospital
• CANS Conference, Washington, DC — Accepted Two Poster Presentations, Dr. Cynthia Chernecky PhD
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TECHNOLOGIES, INC. 32
EFTA01117433
2011 Ililestames Lir rn rri nl i rri tc
July
• VA Hospital, Jackson, MS - Conversion to InVision-Plus - All Lines
• Mayo Clinic, Jacksonville, FL — Straight conversion to InVision-Plus
• VA Hospital, Atlanta, GA - Began InVision-Plus product trial
• Duke University, Oncology Dept., Durham, NC — Began CS product trial (Oncology)
• Sutter Medical Center, Roseville, CA reported zero CR-BSIs for 51/2 years with InVision-Plus
August
• VA Medical Center, San Antonio. TX — Reported "zero" CRBSIs in product trials
September
• APIC Conference, Baltimore, MD
. Clinical Poster Presentation — 122,000 Catheter Day Study
. Clinical Poster Presentation — Texas Children's Hospital NICU, Houston, TX
• Danbury Hospital, Danbury, MA conversion to InVision-Plus
October
• AVA Conference — Clinical Poster Presentation — Methodist Extended Care Hospital
• CANS Conference, Washington, DC — Two Poster Presentations, Dr. Cynthia Chernecky PhD
• Duke University, Oncology Dept., Durham, NC — Completed CS product trial — Zero CR-BSIs
• Spaulding Hospital, Cambridge, MA (Partners) — InVision-Plus successful product trial completed
November -December
• Received supply agreement from Mayo Clinics
• Received supply agreement from Partners Alliance in Boston, MA
• U.S. Army purchasing InVision-Plus product line
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n el TECHNOLOGIES, INC 33
EFTA01117434
Strate • is Goals I Quarter. 2012 aoals
Complete $10.0mm Growth Capital Financing
✓ Engage new accounting firm and new audit firm
✓ Hire new Controller and Senior Director, Marketing & Clinical Education
Expand direct sales force and clinical team
✓ Continue ISO Certification documentation to move international by early Q3 2012
✓ Begin semi-automation modification assembly machine project on to improve margins
Explore supply/distribution agreements and/or joint ventures
✓ Continue developing Amerinet relationships across the U.S
Continue Balance Sheet improvement
✓ Begin new Product Development programs to expand product lines
t, TECHNOLOGIES, INC. 34
EFTA01117435
Strate • is Goals mnnrn nnaIc
➢ Expand board to five members
Introduce product lines into targeted international markets
• Expand manufacturing capabilities and improve margins
Execute worldwide sales, marketing & distribution agreements with major IV players
➢ Continue to expand GPO contracts in U.S.
• Further New Product Development programs to expand product lines
Additional participation at industry conventions and analyst presentations
➢ Establish clinical advisory committee
Successfully defend ourselves against ICU Medical litigation cases during 2012
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I - TECHNOLOGIES, INC. 35
EFTA01117436
Potential Risks
Ability to secure growth capital financings as needed
Ability to keep and attract new sales and support team talent
Ability to secure additional GPO contracts
Continue to penetrate Needleless IV Connector markets
Continue to successfully defend against ICU Medical current litigation
cases
Entry of new competition and technologies
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TECHNOLOGIES, INC 36
EFTA01117437
Strategic Growth Capital Finance Plan
Growth Capital Financing: $ 10.0 Million
Use of Proceeds:
Breakdown: Expansion of direct sales force and support personnel
Cost of goods reduction program
Expansion of manufacturing capacities
Expand into targeted international markets,
Increase industry and public market visibility
Infrastructure
InVision-Plus® CST" Expansion
Payoff targeted notes
Laboratory In-Vitro Testing
Assembly Machine Modification
Capital Equipment
ISO Certification/Mark
Patients/Patient Maintenance
Product Development
Litigation Reserve
Working Capital
Total Use of Funds $ 1.75
$ 0.50
$ 2.00
$ 0.10
$ 0.25
$ 0.50
$ 0.06
$ 0.05
$ 0.70
$ 0.80
$ 3.29
$10.00 Million
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EFTA01117438
Summary
• Strong opportunities for high revenue growth:
— 2012 introduction of new transformation InVision-Plus® CS® technology
— New product developments into additional catheter care & maintenance product lines
— Increased standardization by acute care hospitals, long-term care facilities and home infusion
companies, to include PICCs, CVCs, Stopcocks, and PIVs
— Strategic joint venture relationships and sales, marketing & distribution partners
— Geographic expansion into targeted international markets
• Business model is capable of generating high margins (> 65%) and recurring revenue
• High barriers to entry (intellectual property, regulatory, product safety & efficacy features, and
product development expenses) with limited competition and first to market advantage
• Strong executive, clinical, sales, marketing and manufacturing management team
• Continued focus of the FDA on RyMed's competitors products as they relate to increase in CR-BSIs
(catheter-related bloodstream infections)
38 '" TECHNOLOGIES, INC
EFTA01117439
Thank You for IktirrlibmwdlOweitaxnEttizit
39
EFTA01117440
Reference Slides Only
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TECHNOLOGIES, INC 40
EFTA01117441
FDA Alert & Notification Letter
IVA U.S. Food and Drug Administration
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Positive Displacement Needieless Connectors and
Bloodstream Infections: Initial Communication
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FDA notifies Infection Control
Officer's and Manufacturers via
the ALERT & NOTIFICATION
LETTER on Positive
Displacement I.V. Connectors
RyMed is the ONLY
manufacturer not sited in this
FDA Alert
41
EFTA01117442
Negative Fluid Displacement * * BiofiIm Colonization * *
RyMed's InVision-Plus® in-vitro test study results:
93.0% - 99.9 % reduction of biofilm colonization over other
Competitive I.V. connectors tested
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TECHNOLOGIES, NC. 42
EFTA01117443
Key Product Design Issues ** Septum Seal Integrity * *
Large gaps, openings or certain septum surface designs compromise nursing swabbing and disinfection
practice and contribute to downstream microbial ingress and biofilm colonization potential
Before Swabbing After Aggressive Swabbing After Disconnect
Product shown is currently one of the market leaders
RvNled - InVision-Plus® with Neutral Advantage"'
A fully compressed and tightly sealed septum surface design is important to fully support nursing
swabbing and disinfection practice for effective downstream microbial ingress and biofilm colonization
lEr a:
After 5 Second Swab After Disconnect
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EFTA01117444
Key Product Design Issues **Fluid Pathwa **
Most competitive I.V. connectors have large fluid dead space within the fluid pathway.
Dead space entraps the patient's blood, contributing to biofilm colonization
CareFusion B. Braun
SmartSite® UltraSite® CareFusion®
MaxClearTM
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RyMed - InVision-Plus® with Neutral Advantage"'
Straight-through fluid pathway
Zero dead space
Zero fluid displacement
Low priming volume (0.027mL)
99.94% effective blood clearing after 1 ml normal saline
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TECHNOLOGIES, INC. 44
EFTA01117445
📷 Images in this document (44 detected; 6 largest described)
AI-generated factual descriptions of embedded images (llava:13b). These are searchable across the corpus.
[Image 1] The image shows a poster with various sections of text and graphics. The central theme appears to be related to medical or healthcare data, specifically mentioning "CATHETER DAYS OF AGGREGATED DATA" and "2014 ASSOCIATION FOR PROFESSIONAL INFECTION CONTROL AND EPIIDEMIOLOGY (APIC) CONFERENCE."
On the left side of the poster, there is a graph with a title "CATHETER DAYS OF AGGREGATED DATA" and a su
[Image 2] The image appears to be a screenshot from a presentation or a web page. It contains two photographs side by side, each showing a person's hands manipulating a red object that looks like a coil or a piece of wire. The person's hands are wearing gloves, suggesting a medical or laboratory setting.
Above the photographs, there is a title that reads "The advantage is clear statement." Below the title,
[Image 3] The image shows a screenshot of a webpage with a blue header that reads "FDA Alert & Notification Letter." Below the header is a section titled "JULY 2010" with a subtitle "FDA NOTIFICATIONS INFECTION CONTROL." The main content of the screenshot is a text excerpt from a webpage, which appears to be a letter from the FDA (Food and Drug Administration) regarding infection control. The text includes
[Image 4] The image shows a presentation slide with a blue background and text. The slide is titled "RJR's Competitors' Clinical Infectious Diseases 2009-2012." Below the title, there is a photograph of a document with text that appears to be an article or report from the journal "Clinical Infectious Diseases." The visible text on the document includes phrases such as "RJR's Competitors," "Clinical Infectio
[Image 5] The image displays an infographic with a diagram of a medical device, specifically a catheter. The diagram is labeled with various features and benefits of the device, such as "Neutral Advantage Technology," "RyMed's 10-Point Standard," and "Patented Zero Fluid Displacement." The catheter is shown in a cross-sectional view, highlighting its design elements like the balloon, the shaft, and the hub.
[Image 6] The image is a photograph of a presentation slide with a purple background and a list of names and titles. The slide is titled "MANAGEMENT TEAM" and includes the names, titles, and years of experience for four individuals. The names are listed in a vertical column, and each name is followed by a title and a brief description of their experience. The slide also includes a logo at the bottom right c