| Primary Device ID | 20809160194734 |
| NIH Device Record Key | a4866de8-7489-4397-8bae-6cb4f51e0c2b |
| Commercial Distribution Discontinuation | 2019-04-03 |
| Commercial Distribution Status | Not in Commercial Distribution |
| Brand Name | AVIDTruCustom |
| Version Model Number | VAMM036-05 |
| Company DUNS | 092364462 |
| Company Name | MEDICAL ACTION INDUSTRIES INC. |
| Device Count | 1 |
| DM Exempt | true |
| Pre-market Exempt | true |
| MRI Safety Status | Labeling does not contain MRI Safety Information |
| Human Cell/Tissue Product | false |
| Device Kit | true |
| Device Combination Product | true |
| 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 | true |
| RX Perscription | false |
| OTC Over-The-Counter | true |
| Special Storage Condition, Specify | Between 0 and 0 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 10809160194737 [Primary] |
| GS1 | 20809160194734 [Package] Contains: 10809160194737 Package: [20 Units] Discontinued: 2019-04-03 Not in Commercial Distribution |
| NSB | Patient personal hygiene kit |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2019-04-04 |
| Device Publish Date | 2018-05-17 |
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| 20809160495039 - Medical Action Industries | 2025-10-01 |
| 20809160494896 - Medical Action Industries | 2025-09-29 |
| 20809160494742 - Medical Action Industries | 2025-09-25 |
| 20809160494759 - Medical Action Industries | 2025-09-25 |
| 20809160493905 - Medical Action Industries | 2025-09-16 |
| 20809160493585 - Medical Action Industries | 2025-09-12 |