MTG Jiffy Cath® Mini-Pak

GUDID 10851593006729

Pre - Lubricated Closed System Intermittent Catheter

MEDICAL TECHNOLOGIES OF GEORGIA, INC.

Single-administration urethral catheterization kit, single-use
Primary Device ID10851593006729
NIH Device Record Keyf42c4ec1-ba29-49f0-a092-fbd35ce86345
Commercial Distribution StatusIn Commercial Distribution
Brand NameMTG Jiffy Cath® Mini-Pak
Version Model Number10112
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 Kitfalse
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 Gauge12 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
GS100851593006722 [Primary]
GS110851593006729 [Package]
Contains: 00851593006722
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 Date2019-04-18
Device Publish Date2019-04-10

On-Brand Devices [MTG Jiffy Cath® Mini-Pak]

10851593006743Pre-Lubricated Closed System Intermittent Catheter
10851593006736Pre-Lubricated Closed System Intermittent Catheter
10851593006729Pre - Lubricated Closed System Intermittent Catheter

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