Primary Device ID | 05407010126341 |
NIH Device Record Key | 6cd4ff13-540e-41f2-88e2-3dddf1861958 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Mod ProCHO 5 pwd w/ L-Gln, wo NaHCO3 10L |
Version Model Number | BESP588D |
Catalog Number | BESP588D |
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 |