| Primary Device ID | 03661540202902 |
| NIH Device Record Key | 18cba250-0a6e-47fb-8bc3-86c5e9c04940 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | ENVOY 500 LDL CALIBRATOR KIT |
| Version Model Number | 55115 |
| Company DUNS | 267732378 |
| Company Name | ELITECH CLINICAL SYSTEMS SAS |
| 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 | true |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 03661540202902 [Primary] |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2024-09-16 |
| Device Publish Date | 2016-09-24 |
| 03661540200809 - ENVOY 500 ALT REAGENT KIT | 2024-09-16 |
| 03661540201905 - ENVOY 500 CREATININE REAGENT KIT | 2024-09-16 |
| 03661540202506 - ENVOY 500 ISE BASELINE SOLUTION KIT | 2024-09-16 |
| 03661540202605 - ENVOY 500 ISE CALIBRATOR KIT | 2024-09-16 |
| 03661540202803 - ENVOY 500 ISE REFERENCE SOLUTION KIT | 2024-09-16 |
| 03661540202902 - ENVOY 500 LDL CALIBRATOR KIT | 2024-09-16 |
| 03661540202902 - ENVOY 500 LDL CALIBRATOR KIT | 2024-09-16 |
| 03661540203602 - ENVOY 500 TOTAL PROTEIN REAGENT KIT | 2024-09-16 |
| 03661540203800 - ENVOY 500 BUN REAGENT KIT | 2024-09-16 |