Primary Device ID | 10851593006453 |
NIH Device Record Key | f27da83a-1f5e-4f46-8b46-030c4f176709 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | MTG Instant Cath® Soft / Coude |
Version Model Number | 22712 |
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 | true |
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 |
Phone | 770-788-0763 |
MTGcustomerservice@medtechga.com |
Catheter Gauge | 12 French |
Special Storage Condition, Specify | Between 0 and 0 *Keep Dry , Keep away from direct sunlight |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00851593006456 [Primary] |
GS1 | 10851593006453 [Package] Contains: 00851593006456 Package: [100 Units] In Commercial Distribution |
KOD | Catheter, Urological |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2018-11-09 |
Device Publish Date | 2018-10-09 |
10851593006460 | Pre-Lubricated Closed System Intermittent Catheter - Kit |
10851593006453 | Pre-Lubricated Closed System Intermittent Catheter - Kit |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
MTG INSTANT CATH 77208411 3509572 Live/Registered |
MEDICAL TECHNOLOGIES OF GEORGIA, INC. 2007-06-18 |