Primary Device ID | 20851593006092 |
NIH Device Record Key | 10bc82ae-31e3-4bb1-89f8-bc380159833b |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | MTG Intermittent Catheter, Straight-tip |
Version Model Number | 71114 |
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 | 14 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 | 00851593006098 [Primary] |
GS1 | 10851593006095 [Package] Contains: 00851593006098 Package: [30 Units] In Commercial Distribution |
GS1 | 20851593006092 [Package] Contains: 10851593006095 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 |
20851593006108 | Intermittent Catheter, Straight-tip |
20851593006092 | Intermittent Catheter, Straight-tip |
20851593006085 | Intermittent Catheter, Straight-tip |