Primary Device ID | 00840075404194 |
NIH Device Record Key | 98d4b559-f55a-4898-b63c-85bf095b08ae |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Formulation Buffer (pH 7.40 + 0.20) |
Version Model Number | 04-1250Q (00307661) |
Catalog Number | 04-1250Q (00307661) |
Company DUNS | 609095955 |
Company Name | Lonza Walkersville, Inc. |
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 |