Cystoscopy adaptor

GUDID 04059082030494

SOPRO-COMEG GmbH

Rigid endoscope obturator
Primary Device ID04059082030494
NIH Device Record Key9d8ce6f0-d617-4e47-aa97-77d1ce499174
Commercial Distribution StatusIn Commercial Distribution
Brand NameCystoscopy adaptor
Version Model Number196 810 111
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 Numbertrue
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
GS104059082030494 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

FAJCystoscope and accessories, flexible/rigid

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[04059082030494]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number2
Public Version Date2018-07-06
Device Publish Date2018-03-20

On-Brand Devices [Cystoscopy adaptor]

04059082030654198 050 300
04059082030647198 050 200
04059082030630198 050 100
04059082030500196 810 150
04059082030494196 810 111
04059082030470196 800 150
04059082030319196 050 300
04059082030302196 050 200
04059082030296196 050 100
04059082010588198 050 300BC
04059082010571198 050 200BC
04059082010564198 050 100BC
04059082010397196 810 150BC
04059082010380196 810 111BC
04059082010342196 800 150BC
04059082010144196 050 300BC
04059082010137196 050 200BC
04059082010120196 050 100BC

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