Primary Device ID | 04033817900979 |
NIH Device Record Key | 85ba2c72-8ad3-4b9f-86c4-d78a020e5ab0 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | SCP |
Version Model Number | Emergency Drive Unit |
Company DUNS | 343225272 |
Company Name | LivaNova Deutschland GmbH |
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 | true |
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 |