Obturator

GUDID 04059082010892

SOPRO-COMEG GmbH

Rigid endoscope obturator
Primary Device ID04059082010892
NIH Device Record Key04b545dd-8131-484b-a60e-b4dd320188d7
Commercial Distribution StatusIn Commercial Distribution
Brand NameObturator
Version Model Number199 080 000BC
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
GS104059082010892 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

FDCRESECTOSCOPE, WORKING ELEMENT

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[04059082010892]

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 [Obturator]

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