Primary Device ID | 10803622105057 |
NIH Device Record Key | 087c1c53-a17f-4eac-95f6-3830709669e8 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Arterial cardiopulmonary bypass cannula |
Version Model Number | RA-xxxxx |
Company DUNS | 080914995 |
Company Name | LIVANOVA USA, INC. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | MR Unsafe |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |