Primary Device ID | 05407010124804 |
NIH Device Record Key | c9cc5ae9-a368-47e5-8f0b-f7200d9491ce |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | GLS Lonza Medium Base 4 - 20kg |
Version Model Number | BESP1302X20 |
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 |