Primary Device ID | 10888234500506 |
NIH Device Record Key | e6abfeb6-7848-456c-951f-5b26f1b7d5bb |
Commercial Distribution Discontinuation | 2018-01-15 |
Commercial Distribution Status | Not in Commercial Distribution |
Brand Name | Negative Serum Control |
Version Model Number | 404572 |
Catalog Number | 404572 |
Company DUNS | 606034197 |
Company Name | IMMUCOR GTI DIAGNOSTICS, 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 | false |
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 |