Primary Device ID | 10190302007481 |
NIH Device Record Key | 9462f091-bb55-43ae-8566-75b6a7785c09 |
Commercial Distribution Discontinuation | 2022-04-27 |
Commercial Distribution Status | Not in Commercial Distribution |
Brand Name | AEC Single Solution |
Version Model Number | 001122 |
Company DUNS | 080131636 |
Company Name | LIFE TECHNOLOGIES CORPORATION |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
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 | true |
OTC Over-The-Counter | false |