MTG Female Intermittent Catheter, Straight-tip with hyorphilic low-friction coat

GUDID 20851593006214

Female Intermittent Catheter, Straight-tip with hydrophilic coating

MEDICAL TECHNOLOGIES OF GEORGIA, INC.

Single-administration urethral catheterization kit, single-use

• Primary Device ID: 20851593006214
• NIH Device Record Key: 1e8f66e0-2019-4739-a5f0-fe2dbbc2d70e
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: MTG Female Intermittent Catheter, Straight-tip with hyorphilic low-friction coat
• Version Model Number: 81412
• Company DUNS: 011005491
• Company Name: MEDICAL TECHNOLOGIES OF GEORGIA, INC.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: 770-788-0763
• Email: MTGcustomerservice@medtechga.com

Operating and Storage Conditions

• Special Storage Condition, Specify: Between 0 and 0 *Keep dry; Keep away from direct sunlight
• Special Storage Condition, Specify: Between 0 and 0 *Keep dry; Keep away from direct sunlight

Device Identifiers

Device Issuing Agency	Device ID
GS1	00851593006210 [Primary]
GS1	10851593006217 [Package]; Contains: 00851593006210; Package: [30 Units]; In Commercial Distribution
GS1	20851593006214 [Package]; Contains: 10851593006217; Package: [12 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K111405

FDA Product Code

• GBM: Catheter, Urethral

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: true

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2016-09-13

Devices Manufactured by MEDICAL TECHNOLOGIES OF GEORGIA, INC.

• 00851593006951 - MTG Jiffy Cath™ Coude - PVP kit: 2019-11-07 Pre-Lubricated Closed System Intermittent Catheter - Kit
• 10851593006750 - MTG Jiffy Cath™ Mini-Pak: 2019-09-18 Pre-Lubricated Closed System Intermittent Catheter
• 10851593006767 - MTG Jiffy Cath™ Mini-Pak: 2019-09-18 Pre-Lubricated Closed System Intermittent Catheter
• 10851593006774 - MTG Jiffy Cath™ Mini-Pak: 2019-09-18 Pre-Lubricated Closed System Intermittent Catheter
• 10851593006781 - MTG Jiffy Cath™: 2019-09-18 Pre- Lubricated Closed System Intermittent Catheter
• 10851593006798 - MTG Jiffy Cath™: 2019-09-18 Pre-Lubricated Closed System Intermittent Catheter
• 10851593006804 - MTG Jiffy Cath™: 2019-09-18 Pre-Lubricated Closed System Intermittent Catheter
• 10851593006811 - MTG Jiffy Cath™ Coude: 2019-09-18 Pre-Lubricated Closed System Intermittent Catheter