| Primary Device ID | 20851593006085 |
| NIH Device Record Key | fdeb6f91-029e-474d-a7f3-857b9c2feeb2 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | MTG Intermittent Catheter, Straight-tip |
| Version Model Number | 71112 |
| 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 |
| Special Storage Condition, Specify | Between 0 and 0 *Keep dry; Keep away from direct sunlight |
| Special Storage Condition, Specify | Between 0 and 0 *Keep dry; Keep away from direct sunlight |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00851593006081 [Primary] |
| GS1 | 10851593006088 [Package] Contains: 00851593006081 Package: [30 Units] In Commercial Distribution |
| GS1 | 20851593006085 [Package] Contains: 10851593006088 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 |