Primary Device ID | 10851593006040 |
NIH Device Record Key | 8c7ffdd8-648d-473a-acc4-557ce5d1664e |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | MTG EZ-Advancer® Soft |
Version Model Number | 31214 |
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 | 14 French |
Special Storage Condition, Specify | Between 0 and 0 *Keep Dry , Keep away from direct sunlight |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00851593006043 [Primary] |
GS1 | 10851593006040 [Package] Contains: 00851593006043 Package: [100 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 | 2016-09-13 |
10851593006040 | Pre-Lubricated Closed System Intermittent Catheter - Kit |
10851593006033 | Pre-Lubricated Closed System Intermittent Catheter - Kit |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
MTG EZ-ADVANCER 77722893 3815525 Dead/Cancelled |
Medical Technologies Of Georgia, Inc. 2009-04-27 |