Primary Device ID | 10803622103718 |
NIH Device Record Key | a321d2a6-2f52-453c-bf39-bb14837a312e |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Cardioplegia solution administration adaptor |
Version Model Number | CA-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 | 00803622103711 [Primary] |
GS1 | 10803622103718 [Package] Contains: 00803622103711 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 | 3 |
Public Version Date | 2018-08-15 |
Device Publish Date | 2015-07-16 |
10803622106634 | CA-xxxxx |
10803622106627 | CA-xxxxx |
10803622106610 | CA-xxxxx |
10803622103794 | CA-xxxxx |
10803622103787 | CA-xxxxx |
10803622103770 | CA-xxxxx |
10803622103763 | CA-xxxxx |
10803622103756 | CA-xxxxx |
10803622103749 | CA-xxxxx |
10803622103732 | CA-xxxxx |
10803622103725 | CA-xxxxx |
10803622103718 | CA-xxxxx |
10803622103701 | CA-xxxxx |
10803622103695 | CA-xxxxx |
10803622103688 | CA-xxxxx |
10803622103671 | CA-xxxxx |
10803622103664 | CA-xxxxx |
10803622103657 | CA-xxxxx |
10803622103640 | CA-xxxxx |
10803622103633 | CA-xxxxx |
10803622103626 | CA-xxxxx |
10803622103619 | CA-xxxxx |
10803622103602 | CA-xxxxx |