Primary Device ID | 20851593006269 |
NIH Device Record Key | 29eb057e-9ca4-4c58-bebf-c379a90225ee |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | MTG Pediatric Intermittent Catheter, Coude-tip |
Version Model Number | 71610 |
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 | 10 French |
Special Storage Condition, Specify | Between 0 and 0 *Storage temperature not to exceed 120 degrees Fahrenheit |
Special Storage Condition, Specify | Between 0 and 0 *Storage temperature not to exceed 120 degrees Fahrenheit |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00851593006265 [Primary] |
GS1 | 10851593006262 [Package] Contains: 00851593006265 Package: [30 Units] In Commercial Distribution |
GS1 | 20851593006269 [Package] Contains: 10851593006262 Package: [12 Units] In Commercial Distribution |
GBM | Catheter, Urethral |
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 |
20851593006269 | Pediatric Intermittent Catheter, Coude-tip |
20851593006252 | Pediatric Intermittent Catheter, Coude-tip |