Arthroscope Bridge

GUDID 04059082007243

SOPRO-COMEG GmbH

Endoscope sheath, reusable
Primary Device ID04059082007243
NIH Device Record Key0d6f620a-5983-4998-9cdc-19d4aca7f3bd
Commercial Distribution StatusIn Commercial Distribution
Brand NameArthroscope Bridge
Version Model Number191 401 781
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
GS104059082007243 [Primary]

FDA Product Code

HRXArthroscope

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[04059082007243]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2019-03-11
Device Publish Date2018-04-12

Devices Manufactured by SOPRO-COMEG GmbH

04059082003559 - Thoracoscope2019-11-08
04059082003757 - Hysteroscope2019-11-08
04059082003764 - Hysteroscope2019-11-08
04059082003795 - Hysteroscope2019-11-08
04059082003818 - Hysteroscope2019-11-08
04059082003856 - Hysteroscope2019-11-08
04059082003870 - Hysteroscope2019-11-08
04059082003894 - Hysteroscope2019-11-08

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