Bipolar HF cable

GUDID 04059082012919

SOPRO-COMEG GmbH

Electrical-only medical device connection cable, reusable
Primary Device ID04059082012919
NIH Device Record Keyf3b99787-06dd-4873-a124-e63b6156cf32
Commercial Distribution StatusIn Commercial Distribution
Brand NameBipolar HF cable
Version Model Number390 805 000
Company DUNS507185952
Company NameSOPRO-COMEG GmbH
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 Usefalse
Lot Batchtrue
Serial Numberfalse
Manufacturing Datetrue
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS104059082012919 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

FASELECTRODE, ELECTROSURGICAL, ACTIVE, UROLOGICAL

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[04059082012919]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2018-07-06
Device Publish Date2016-09-12

On-Brand Devices [Bipolar HF cable]

04059082013039390 865 000
04059082013022390 863 000
04059082012995390 845 000
04059082012988390 843 000
04059082012971390 835 000
04059082012964390 833 000
04059082012957390 825 000
04059082012940390 823 000
04059082012933390 815 000
04059082012926390 813 000
04059082012919390 805 000
04059082012902390 803 000

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