Bipolar electrode

GUDID 04059082014661

SOPRO-COMEG GmbH

Laparoscopic grasping forceps, reusable
Primary Device ID04059082014661
NIH Device Record Keyc4f636ea-22a9-4488-bc50-d40d31cb7b3e
Commercial Distribution StatusIn Commercial Distribution
Brand NameBipolar electrode
Version Model Number392 993 014
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
GS104059082014661 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

GCJLaparoscope, general & plastic surgery

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[04059082014661]

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 electrode]

04059082014883392 993 127
04059082014876392 993 126
04059082014869392 993 125
04059082014661392 993 014
04059082014654392 993 013
04059082014630392 993 011
04059082014623392 993 010
04059082014616392 993 009
04059082014609392 993 008

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