Primary Device ID | 00854515008477 |
NIH Device Record Key | b89ddbbd-2f04-43cd-8a6a-bdd34cec1736 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | MI Broach Handle |
Version Model Number | Posterior |
Catalog Number | 01.10.10.462 |
Company DUNS | 079820535 |
Company Name | Unique Surgical |
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 | false |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | false |