Resectoscopy working element

GUDID 04059082031262

SOPRO-COMEG GmbH

Rigid endoscope working guide
Primary Device ID04059082031262
NIH Device Record Key6b0cfcd7-1949-45c5-9bd3-f44f5cf415c4
Commercial Distribution StatusIn Commercial Distribution
Brand NameResectoscopy working element
Version Model Number195 010 040
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
GS104059082031262 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

FDCRESECTOSCOPE, WORKING ELEMENT

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[04059082031262]

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 [Resectoscopy working element]

04059082031651199 020 000
04059082031644199 010 020
04059082031606195 810 000
04059082031576195 800 000
04059082031545195 400 000
04059082031293195 020 050
04059082031286195 020 040
04059082031279195 020 000
04059082031262195 010 040
04059082031255195 010 000
04059082025391395 015 002
04059082025384395 015 001
04059082010687199 020 000BC
04059082010656199 010 020BC
04059082009780195 810 000BC
04059082009599195 800 000BC
04059082009506195 400 000BC
04059082008479195 020 050BC
04059082008462195 020 040BC
04059082008431195 020 000BC
04059082008400195 010 040BC
04059082008370195 010 000BC

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