Redfield IRC 2100

GUDID 20888937013249

Contact Tip/Sheath

Coopersurgical, Inc.

Infrared tissue coagulation system handpiece Infrared tissue coagulation system handpiece Infrared tissue coagulation system handpiece Infrared tissue coagulation system handpiece Infrared tissue coagulation system handpiece Infrared tissue coagulation system handpiece Infrared tissue coagulation system handpiece Infrared tissue coagulation system handpiece Infrared tissue coagulation system handpiece Infrared tissue coagulation system handpiece Infrared tissue coagulation system handpiece Infrared tissue coagulation system handpiece Infrared tissue coagulation system handpiece Infrared tissue coagulation system handpiece Infrared tissue coagulation system handpiece Infrared tissue coagulation system handpiece Infrared tissue coagulation system handpiece Infrared tissue coagulation system handpiece Infrared tissue coagulation system handpiece Infrared tissue coagulation system handpiece Infrared tissue coagulation system handpiece Infrared tissue coagulation system handpiece Infrared tissue coagulation system handpiece Infrared tissue coagulation system handpiece Infrared tissue coagulation system handpiece Infrared tissue coagulation system handpiece Infrared tissue coagulation system handpiece Infrared tissue coagulation system handpiece Infrared tissue coagulation system handpiece Infrared tissue coagulation system handpiece Infrared tissue coagulation system handpiece
Primary Device ID20888937013249
NIH Device Record Key8884d132-e50a-4ca8-a319-47cc6a008d3a
Commercial Distribution StatusIn Commercial Distribution
Brand NameRedfield IRC 2100
Version Model NumberRIRC-DT6120
Company DUNS801895244
Company NameCoopersurgical, Inc.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Dimensions

Outer Diameter6 Millimeter
Length120 Millimeter
Outer Diameter6 Millimeter
Length120 Millimeter
Outer Diameter6 Millimeter
Length120 Millimeter
Outer Diameter6 Millimeter
Length120 Millimeter
Outer Diameter6 Millimeter
Length120 Millimeter
Outer Diameter6 Millimeter
Length120 Millimeter
Outer Diameter6 Millimeter
Length120 Millimeter
Outer Diameter6 Millimeter
Length120 Millimeter
Outer Diameter6 Millimeter
Length120 Millimeter
Outer Diameter6 Millimeter
Length120 Millimeter
Outer Diameter6 Millimeter
Length120 Millimeter
Outer Diameter6 Millimeter
Length120 Millimeter
Outer Diameter6 Millimeter
Length120 Millimeter
Outer Diameter6 Millimeter
Length120 Millimeter
Outer Diameter6 Millimeter
Length120 Millimeter
Outer Diameter6 Millimeter
Length120 Millimeter
Outer Diameter6 Millimeter
Length120 Millimeter
Outer Diameter6 Millimeter
Length120 Millimeter
Outer Diameter6 Millimeter
Length120 Millimeter
Outer Diameter6 Millimeter
Length120 Millimeter
Outer Diameter6 Millimeter
Length120 Millimeter
Outer Diameter6 Millimeter
Length120 Millimeter
Outer Diameter6 Millimeter
Length120 Millimeter
Outer Diameter6 Millimeter
Length120 Millimeter
Outer Diameter6 Millimeter
Length120 Millimeter
Outer Diameter6 Millimeter
Length120 Millimeter
Outer Diameter6 Millimeter
Length120 Millimeter
Outer Diameter6 Millimeter
Length120 Millimeter
Outer Diameter6 Millimeter
Length120 Millimeter
Outer Diameter6 Millimeter
Length120 Millimeter
Outer Diameter6 Millimeter

Device Identifiers

Device Issuing AgencyDevice ID
GS100888937013245 [Primary]
GS120888937013249 [Package]
Contains: 00888937013245
Package: [10 Units]
In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

KNSUnit, Electrosurgical, Endoscopic (With Or Without Accessories)

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2018-07-06
Device Publish Date2016-09-20

On-Brand Devices [Redfield IRC 2100]

20888937013256Contact Tip/Sheath
20888937013249Contact Tip/Sheath

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.