Primary Device ID | 00888707000420 |
NIH Device Record Key | 6d99327e-b490-4f0e-b955-856dc23436fb |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | HVAD® Controller |
Version Model Number | 1420 |
Catalog Number | 1420 |
Company DUNS | 146054536 |
Company Name | Heartware 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 | false |
Serial Number | true |
Manufacturing Date | true |
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 | 00888707000420 [Primary] |
DSQ | Ventricular (Assisst) Bypass |
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 | 2017-05-18 |
00888707006859 | 1403US |
00888707000420 | 1420 |
00888707007658 | 1420 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
HVAD 85758552 not registered Dead/Abandoned |
HeartWare Inc. 2012-10-19 |
HVAD 78910214 3730135 Live/Registered |
HeartWare, Inc. 2006-06-16 |