Primary Device ID | 03661540202605 |
NIH Device Record Key | 7a790a11-663c-43b0-8642-adffd1f99b71 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | ENVOY 500 ISE CALIBRATOR KIT |
Version Model Number | 55117 |
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 | 03661540202605 [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 |
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 |
03661540203602 - ENVOY 500 TOTAL PROTEIN REAGENT KIT | 2024-09-16 |
03661540203800 - ENVOY 500 BUN REAGENT KIT | 2024-09-16 |