Primary Device ID | 00886799000120 |
NIH Device Record Key | b45f05dd-b680-48a9-9c3c-36750e27a34c |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Sarns™ Centrifugal System |
Version Model Number | 9490 |
Catalog Number | 9490 |
Company DUNS | 177655466 |
Company Name | Terumo Cardiovascular Systems Corporation |
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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00886799000120 [Primary] |
KFM | Pump, Blood, Cardiopulmonary Bypass, Non-Roller Type |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2015-09-24 |
00886799001714 | Spare Pump Power Cord for the Centrifugal Pump Back-Up Battery. |
00886799000120 | Centrifugal Pump Back-Up Battery |
00886799000076 | Centrifugal Pump Speed Control Module |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
SARNS 86271501 not registered Dead/Abandoned |
Terumo Cardiovascular Systems Corporation 2014-05-05 |
SARNS 73676567 1480452 Dead/Cancelled |
AMERICAN ANCHOR, INC. 1987-07-30 |
SARNS 72305072 0880541 Live/Registered |
SARNS, INC. 1968-08-13 |