| Primary Device ID | 20809160106508 |
| NIH Device Record Key | 7b655d01-0a5e-4c4b-9ac0-61fd9bf328aa |
| Commercial Distribution Discontinuation | 2019-09-30 |
| Commercial Distribution Status | Not in Commercial Distribution |
| Brand Name | TRA MEDICAL AND DENTAL SUPPLY |
| Version Model Number | 70226 |
| 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 | 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 | true |
| RX Perscription | false |
| OTC Over-The-Counter | true |
| Special Storage Condition, Specify | Between 0 and 0 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 10809160106501 [Primary] |
| GS1 | 20809160106508 [Package] Contains: 10809160106501 Package: [50 Units] Discontinued: 2019-09-30 Not in Commercial Distribution |
| MCZ | Suture removal kit |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2019-10-01 |
| Device Publish Date | 2016-09-22 |
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