Urology syringe

GUDID 04059082008974

SOPRO-COMEG GmbH

General-purpose syringe, reusable
Primary Device ID04059082008974
NIH Device Record Key0949e836-1365-435d-9b2f-bd77b2f221a7
Commercial Distribution StatusIn Commercial Distribution
Brand NameUrology syringe
Version Model Number195 090 302
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
GS104059082008974 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

FJLRESECTOSCOPE

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[04059082008974]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number4
Public Version Date2018-09-12
Device Publish Date2016-09-12

On-Brand Devices [Urology syringe]

04059082032061199 090 200
04059082032054199 090 100
04059082032030195 091 000
04059082032023195 090 200
04059082032016195 090 100
04059082025513395 015 033
04059082025506395 015 032
04059082010915199 090 200 C
04059082010908199 090 100 C
04059082009032195 091 000BC
04059082008974195 090 302
04059082008967195 090 301
04059082008950195 090 300
04059082008943195 090 200 C
04059082008929195 090 100 C

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