| Primary Device ID | 00817238010479 |
| NIH Device Record Key | 8766bceb-db4c-4793-ae4f-bac7f7a06747 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Alcohol/Ammonia Control Bi-level |
| Version Model Number | 95505 |
| Company DUNS | 078742335 |
| Company Name | CLINIQA CORPORATION |
| 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 | true |
| Device Combination Product | false |
| Single Use | false |
| 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 | 00817238010479 [Primary] |
| JJY | Multi-Analyte Controls, All Kinds (Assayed) |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2019-02-04 |
| Device Publish Date | 2018-08-22 |
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