| Primary Device ID | 00860013131265 |
| NIH Device Record Key | a77d33a0-6a36-44be-96b8-1812aab2625c |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Genetic Testing - Saliva IG |
| Version Model Number | 136350 |
| Company DUNS | 114193536 |
| Company Name | Medzah Industries |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | true |
| 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 | false |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00860013131265 [Primary] |
| NNK | Container, Specimen Mailer And Storage, Non-Sterile |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2024-12-05 |
| Device Publish Date | 2024-11-27 |
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