Primary Device ID | 10850003761081 |
NIH Device Record Key | 407f9670-f280-4a69-bf41-1489c6894d74 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Qunatra QPlus System |
Version Model Number | KT-0034 |
Company DUNS | 193921041 |
Company Name | HEMOSONICS, LLC |
Device Count | 4 |
DM Exempt | true |
Pre-market Exempt | false |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | true |
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 |