| Primary Device ID | 84014501003431 |
| NIH Device Record Key | e8769cb8-eaac-44b2-af78-e4671a932659 |
| Commercial Distribution Discontinuation | 2019-07-16 |
| Commercial Distribution Status | Not in Commercial Distribution |
| Brand Name | Cosmolux Lynx K1 |
| Version Model Number | FR75 T12 180W SM |
| Catalog Number | 26503 |
| Company DUNS | 330119702 |
| Company Name | NARVA Lichtquellen GmbH + Co KG. |
| 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 | false |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | true |
| 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 | true |
| Phone | +1 781 331 0949 |
| info@jwnorthamerica.com |
| Special Storage Condition, Specify | Between 0 and 0 *Keep dry. Attention: Fragile. |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 04014501003435 [Primary] |
| GS1 | 54014501403438 [Package] Contains: 04014501003435 Package: Tertiary Packaging [24 Units] Discontinued: 2019-07-16 Not in Commercial Distribution |
| GS1 | 84014501003431 [Package] Contains: 54014501403438 Package: Pallet [24 Units] Discontinued: 2019-07-16 Not in Commercial Distribution |
| LEJ | Booth, Sun Tan |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2019-07-18 |
| Device Publish Date | 2017-12-13 |
| 84014501003431 | FR75 T12 180W SM |
| 54014501404121 | FR75 T12 180-200W SM |
| 54014501505194 | FR75 T12 180-200W SM |