Primary Device ID | 10851593006392 |
NIH Device Record Key | a33c5409-dfee-46ee-b04d-f4720c7f770b |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | MTG EZ-Gripper® Long |
Version Model Number | 50816 |
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 |
Phone | 770-788-0763 |
MTGcustomerservice@medtechga.com |
Catheter Gauge | 16 French |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00851593006395 [Primary] |
GS1 | 10851593006392 [Package] Contains: 00851593006395 Package: [50 Units] In Commercial Distribution |
KOD | Catheter, Urological |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2017-08-10 |
10851593006422 | Pre-Lubricated Closed System Intermittent Catheter-Kit |
10851593006415 | Pre-Lubricated Closed System Intermittent Catheter-Kit |
10851593006408 | Pre-Lubricated Closed System Intermittent Catheter-Kit |
10851593006392 | Pre-Lubricated Closed System Intermittent Catheter 18in long |
10851593006385 | Pre-Lubricated Closed System Intermittent Catheter 18in Long |
10851593006378 | Pre-Lubricated Closed System Intermittent Catheter 18in long |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
MTG EZ-GRIPPER 77622502 3694056 Live/Registered |
Medical Technologies Of Georgia, Inc. 2008-11-26 |