Bipolar forceps

GUDID 04059082014722

SOPRO-COMEG GmbH

Laparoscopic grasping forceps, reusable
Primary Device ID04059082014722
NIH Device Record Key6b71a3d7-eb0f-4e34-8608-fa04ebebffe2
Commercial Distribution StatusIn Commercial Distribution
Brand NameBipolar forceps
Version Model Number392 993 021
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
GS104059082014722 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

GCJLaparoscope, general & plastic surgery

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[04059082014722]

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 forceps]

04059082014852392 993 124
04059082014821392 993 121
04059082014814392 993 119
04059082014807392 993 118
04059082014791392 993 117
04059082014753392 993 024
04059082014722392 993 021
04059082014715392 993 019
04059082014708392 993 018
04059082014692392 993 017
04059082014579392 993 003
04059082014562392 993 002
04059082014555392 993 001

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