Primary Device ID | 05407010127843 |
NIH Device Record Key | 11a48a7f-0126-4980-b128-3e713739c259 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | KH-020 BF-B - 1L Bag SAMPLE |
Version Model Number | BESP1616P1SAM |
Catalog Number | BESP1616P1SAM |
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 |