Primary Device ID | 00821925031210 |
NIH Device Record Key | d3591296-1f0d-42ac-bcf0-b58c378ecf1b |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | ULTRATRACK Hybrid Guidewire 0.038" (0.97mm) x 150cm Regular Body, 3cm |
Version Model Number | GWH3805RA |
Company DUNS | 007198742 |
Company Name | Gyrus Acmi, Inc. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
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 |