Primary Device ID | 28717648013922 |
NIH Device Record Key | 20e819bd-2dc5-4730-810f-a01daf5b9b34 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | TORQUE DEVICE |
Version Model Number | 1003279 |
Catalog Number | 1003279 |
Company DUNS | 964569052 |
Company Name | ABBOTT VASCULAR 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 |