Primary Device ID | 00840861101009 |
NIH Device Record Key | 4a030c7f-0ea0-4034-844d-74ecfd0c9b7e |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Dry Acid Dissolution Unit |
Version Model Number | 160148 |
Company DUNS | 076594100 |
Company Name | Fresenius Usa, Inc. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
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 | true |
Manufacturing Date | false |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |