hamburger-nav-icon
region-flag-icon
Search by Category
Audio
Cameras
Cases & Bags
Computers & Software
Conferencing
Content Management
Control
Displays
Furniture
Lighting & Studio
Mounts & Rigging
Networking & Cabling
Power
Presentation
Production & Lighting
Security & Safety
Signal Management
Search by Category
EnglishFrenchGermanItalianPortugueseSpanish
purelink
Request
More Information
Project List
PureLink’s PureMedia Line Gains FDA Class 1 Clearance - Company's PureMedia Solutions Certified for Use in Patient-Facing Medical Applications
Posted on Tuesday, July 12, 2016
PureLink’s PureMedia Line Gains FDA Class 1 Clearance - Company's PureMedia Solutions Certified for Use in Patient-Facing Medical Applications

PureLink, a leading manufacturer of advanced HD video connectivity solutions, today announced that the U.S. Food and Drug Administration (FDA) has deemed models from its PureMedia line of matrix switchers in compliance with applicable performance and safety standards regarding Electromagnetic Interference (EMI) and Radio-Frequency Interference (RFI) for electronic products. The PureLink devices approved by the agency include all PureMedia matrix switcher chassis, input and output cards, and extenders. Compliance is based on a quality control and testing program which demonstrates that each product manufactured complies with the applicable standard.

The FDA's Center for Devices and Radiological Health (CDRH) compiles an annual Electronic Product Report that accesses and categorizes the radiation safety performance standards of devices from manufacturers that are submitted for approval. Certification means that the manufacturer of a radiation-emitting electronic product states that the product complies with an applicable FDA performance standard and does not emit hazardous and unnecessary radiation. Examples of non-medical electronic products covered by these standards include television receivers and monitors, video displays, entertainment lasers, cordless and cellular telephones, laser CD players and other related equipment and devices.

"This acknowledgement by the FDA further validates the stringent quality and safety standards we have always engineered into our products," stated Howard Schilling, PureLink's Director of Sales. "For our customers in the medical and healthcare vertical, this officially authorizes the PureMedia line for use in patient-facing environments such as operating rooms, ICUs, and long-term patient care facilities," he added.

For more information about PureLink’s PureMedia line of HD video and data distribution management solutions, please call 201-488-3232 or go to www.purelinkav.com.

About PureLink

PureLink designs and manufactures the world’s most respected HD Video connectivity solutions, consisting of products such as Cross-Platform Digital Modular and Integrated Matrix Switchers, Presentation Systems, CATx/Fiber Optic Extenders, Format Converters, Video Switchers and Distribution Amplifiers, along with accessories such as Signal Analyzers, Audio Downmixers, Digital Signal Isolators, and DisplayPort, Fiber Optic, and HDMI Cables and Adapters.  Founded in 2002, PureLink has quietly pioneered the exploding HD Video connectivity space, inventing 1080p HDCP matrix switching along with the large-scale DVI Matrix Switcher. For further information on all PureLink product offerings please go to www.purelinkav.com.  

Contact:                                                 
Mike Salerno, Channel Marketing Manager
mike@purelinkav.com
(201) 488-3232

# # #