MTG Intermittent catheter, Straight-tip with hydrophilic low-friction coating.

GUDID 20851593006191

Intermittent Catheter, Straight-tip with hydrophilic coating

MEDICAL TECHNOLOGIES OF GEORGIA, INC.

Single-administration urethral catheterization kit, single-use
Primary Device ID20851593006191
NIH Device Record Key4a4c148e-1fe0-4185-b1c5-b925f393cd4e
Commercial Distribution StatusIn Commercial Distribution
Brand NameMTG Intermittent catheter, Straight-tip with hydrophilic low-friction coating.
Version Model Number81112
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
Special Storage Condition, SpecifyBetween 0 and 0 *Keep dry; Keep away from direct sunlight

Device Identifiers

Device Issuing AgencyDevice ID
GS100851593006197 [Primary]
GS110851593006194 [Package]
Contains: 00851593006197
Package: [30 Units]
In Commercial Distribution
GS120851593006191 [Package]
Contains: 10851593006194
Package: [12 Units]
In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

GBMCatheter, Urethral

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2018-07-06
Device Publish Date2016-09-13

Devices Manufactured by MEDICAL TECHNOLOGIES OF GEORGIA, INC.

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