Primary Device ID | 05407010124583 |
NIH Device Record Key | 19822fdf-8c3e-4efa-b145-e0202c3c93b1 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Bulk Packaged sterile filtered WFI-200L |
Version Model Number | BE02-038P200 |
Catalog Number | BE02-038P200 |
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 |