Aspiration cannula

GUDID 04059082031538

SOPRO-COMEG GmbH

Endoscopic irrigation/aspiration pump
Primary Device ID04059082031538
NIH Device Record Keyd4e8758c-63c3-464b-b65a-550ddbb28815
Commercial Distribution StatusIn Commercial Distribution
Brand NameAspiration cannula
Version Model Number195 200 270
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
GS104059082031538 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

FDCRESECTOSCOPE, WORKING ELEMENT

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[04059082031538]

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 [Aspiration cannula]

04059082031538195 200 270
04059082031507195 200 230
04059082009490195 200 270BC
04059082009469195 200 230BC

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