MTG Jiffy Cath™ Coude

GUDID 10851593006897

Pre-Lubricated Closed System Intermittent Catheter - Kit

MEDICAL TECHNOLOGIES OF GEORGIA, INC.

Single-administration urethral catheterization kit, single-use
Primary Device ID10851593006897
NIH Device Record Keya0a5da70-9ab2-4f0f-8f58-a320944d4309
Commercial Distribution StatusIn Commercial Distribution
Brand NameMTG Jiffy Cath™ Coude
Version Model Number22614
Company DUNS011005491
Company NameMEDICAL TECHNOLOGIES OF GEORGIA, INC.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kittrue
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone770-788-0763
EmailMTGcustomerservice@medtechga.com

Device Dimensions

Catheter Gauge14 French

Operating and Storage Conditions

Special Storage Condition, SpecifyBetween 0 and 0 *Keep Dry , Keep away from direct sunlight

Device Identifiers

Device Issuing AgencyDevice ID
GS100851593006890 [Primary]
GS110851593006897 [Package]
Contains: 00851593006890
Package: [100 Units]
In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

KODCatheter, Urological

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2019-09-18
Device Publish Date2019-09-10

On-Brand Devices [MTG Jiffy Cath™ Coude]

10851593006903Pre-Lubricated Closed System Intermittent Catheter - Kit
10851593006897Pre-Lubricated Closed System Intermittent Catheter - Kit
10851593006880Pre-Lubricated Closed System Intermittent Catheter - Kit

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