Primary Device ID | 08305900070231 |
NIH Device Record Key | dd24682c-899e-4fa0-b3b7-7ba949d67747 |
Commercial Distribution Discontinuation | 2020-07-01 |
Commercial Distribution Status | Not in Commercial Distribution |
Brand Name | ACTH [Adrenocorticotropic Hormone] ELISA |
Version Model Number | 7023 |
Company DUNS | 067647321 |
Company Name | BIOMERICA, INC. |
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 |
Phone | +1 949 645 2111 |
info@biomerica.com | |
Phone | +1 949 645 2111 |
info@biomerica.com | |
Phone | +1 949 645 2111 |
info@biomerica.com | |
Phone | +1 949 645 2111 |
info@biomerica.com | |
Phone | +1 949 645 2111 |
info@biomerica.com | |
Phone | +1 949 645 2111 |
info@biomerica.com | |
Phone | +1 949 645 2111 |
info@biomerica.com | |
Phone | +1 949 645 2111 |
info@biomerica.com | |
Phone | +1 949 645 2111 |
info@biomerica.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 08305900070231 [Primary] |
CKG | Radioimmunoassay, Acth |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2021-09-02 |
Device Publish Date | 2016-12-07 |
00083059070231 | The Biomerica ACTH ELISA is intended for the quantitative determination of ACTH (Adrenocorticotr |
08305900070231 | The Biomerica ACTH ELISA is intended for the quantitative determination of ACTH (Adrenocorticotr |