Trocar sleeve

GUDID 04059082005089

SOPRO-COMEG GmbH

Laparoscopic access cannula, reusable
Primary Device ID04059082005089
NIH Device Record Keye3fda489-05dc-4d94-9f82-9683108cc24f
Commercial Distribution StatusIn Commercial Distribution
Brand NameTrocar sleeve
Version Model Number191 070 080
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
GS104059082005089 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

GCJLaparoscope, general & plastic surgery

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[04059082005089]

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 [Trocar sleeve]

04059082005522191 120 120
04059082005508191 120 090
04059082005492191 120 080
04059082005485191 120 070
04059082005362191 111 110
04059082005355191 111 100
04059082005348191 111 090
04059082005331191 111 080
04059082005324191 111 070
04059082005218191 101 080
04059082005201191 101 070
04059082005089191 070 080
04059082004914191 051 120
04059082004907191 051 110
04059082004891191 051 100
04059082004884191 051 090
04059082004877191 051 080
04059082004860191 051 070
04059082004785191 031 080
04059082004778191 031 070

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