Primary Device ID | 05407010126068 |
NIH Device Record Key | 82d69ef6-4a5d-4a78-bc06-425eb318959b |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | New DMEM SPR_V01 - 500L |
Version Model Number | BESP1200L |
Catalog Number | BESP1200L |
Company DUNS | 370158847 |
Company Name | Lonza Verviers |
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 | false |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | false |