Cystoscopy obturator

GUDID 04059082010618

SOPRO-COMEG GmbH

Rigid endoscope obturator
Primary Device ID04059082010618
NIH Device Record Key9c8f19da-510f-41ec-92d7-1748240a598e
Commercial Distribution StatusIn Commercial Distribution
Brand NameCystoscopy obturator
Version Model Number198 070 400BC
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
GS104059082010618 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

FAJCystoscope and accessories, flexible/rigid

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[04059082010618]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2018-07-06
Device Publish Date2016-12-22

On-Brand Devices [Cystoscopy obturator]

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04059082030678198 070 400
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04059082030616198 040 400
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04059082030586198 040 100
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04059082030241196 040 200
04059082030234196 040 100
04059082025483395 015 030
04059082025476395 015 029
04059082025469395 015 028
04059082010625198 070 500BC
04059082010618198 070 400BC
04059082010601198 070 300BC
04059082010557198 040 500BC
04059082010540198 040 400BC
04059082010533198 040 300BC
04059082010526198 040 200BC
04059082010519198 040 100BC
04059082010335196 800 110BC
04059082010199196 070 400BC
04059082010182196 070 300BC
04059082010175196 070 200BC
04059082010168196 070 100BC
04059082010113196 040 500BC
04059082010106196 040 400BC
04059082010090196 040 301BC
04059082010083196 040 300BC
04059082010076196 040 200BC
04059082010069196 040 100BC

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