| Primary Device ID | 20851593006481 |
| NIH Device Record Key | 1961785e-25a5-476c-99e4-e3da1132418c |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | MTG Soft Intermittent Catheter /Coude W/Indicator Line |
| Version Model Number | 81712 |
| 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 | 12 French |
| Storage Environment Temperature | Between 33 Degrees Fahrenheit and 120 Degrees Fahrenheit |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00851593006487 [Primary] |
| GS1 | 10851593006484 [Package] Contains: 00851593006487 Package: [30 Units] In Commercial Distribution |
| GS1 | 20851593006481 [Package] Contains: 10851593006484 Package: [12 Units] In Commercial Distribution |
| GBM | Catheter, Urethral |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2019-02-25 |
| Device Publish Date | 2019-01-25 |
| 20851593006504 | Intermittent Catheter Coude-tip with hydrophilic low-friction coating and indicator line |
| 20851593006498 | Intermittent Catheter Coude-tip with hydrophilic low-friction coating and indicator line |
| 20851593006481 | Intermittent Catheter Coude-tip with hydrophilic low-friction coating and indicator line |