Primary Device ID | 00840075404125 |
NIH Device Record Key | 0b031abf-e915-44c9-931d-1a5d70102460 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | TE Buffer (pH 7.90 + 0.30) |
Version Model Number | 04-1244Q (00307645) |
Catalog Number | 04-1244Q (00307645) |
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 |