Primary Device ID | 10888234500360 |
NIH Device Record Key | 81c99483-923a-4f7f-94ff-4f43ecd1829c |
Commercial Distribution Discontinuation | 2018-08-01 |
Commercial Distribution Status | Not in Commercial Distribution |
Brand Name | Stopping Solution |
Version Model Number | 403603 |
Catalog Number | 403603 |
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 |