Primary Device ID | 10803622128384 |
NIH Device Record Key | 88e23cdb-2b7d-4808-9d0b-e0e61f55e700 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Assy, Venous Drainage, Cannula Conversion, 3/8 |
Version Model Number | AX-xxxxx |
Company DUNS | 080914995 |
Company Name | LIVANOVA 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 | 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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00803622128387 [Primary] |
GS1 | 10803622128384 [Package] Contains: 00803622128387 Package: CASE [10 Units] In Commercial Distribution |
DTL | Adaptor, stopcock, manifold, fitting, cardiopulmonary bypass |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2018-08-15 |
Device Publish Date | 2015-09-22 |
00803622159039 - Perfusion Pack | 2025-04-04 |
10803622159043 - Perfusion Pack | 2025-04-04 |
10803622159050 - Perfusion Pack | 2025-04-04 |
00803622159060 - Perfusion Pack | 2025-04-04 |
00803622159077 - Perfusion Pack | 2025-04-04 |
00803622159084 - Perfusion Pack | 2025-04-04 |
10803622159111 - Perfusion Pack | 2025-04-04 |
10803622158831 - Perfusion Pack | 2025-04-01 |