Primary Device ID | 10803622103060 |
NIH Device Record Key | c21d7809-10de-4fe9-8201-b91f9e9a7de9 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Cardioplegia cannula |
Version Model Number | AR-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 | 00803622103063 [Primary] |
GS1 | 10803622103060 [Package] Contains: 00803622103063 Package: CASE [10 Units] In Commercial Distribution |
DWF | CATHETER, CANNULA AND TUBING, VASCULAR, 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 | 2015-07-16 |
10803622128353 | AR-xxxxx |
10803622106511 | AR-xxxxx |
10803622106504 | AR-xxxxx |
10803622106252 | VC-xxxxx |
10803622106245 | VC-xxxxx |
10803622106238 | VC-xxxxx |
10803622106221 | VC-xxxxx |
10803622103114 | AR-xxxxx |
10803622103091 | AR-xxxxx |
10803622103084 | AR-xxxxx |
10803622103077 | AR-xxxxx |
10803622103060 | AR-xxxxx |
10803622103053 | AR-xxxxx |
10803622103046 | AR-xxxxx |
10803622103039 | AR-xxxxx |
10803622103022 | AR-xxxxx |
10803622103015 | AR-xxxxx |
10803622103008 | AR-xxxxx |