Primary Device ID | 08033390114523 |
NIH Device Record Key | d0a51ace-7ab6-4fe8-8b48-2eb84eab9b6a |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Bone Screw |
Version Model Number | 9CC0.30.003 |
Catalog Number | 9CC0.30.003 |
Company DUNS | 432066322 |
Company Name | LIMACORPORATE SPA |
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 | true |
OTC Over-The-Counter | false |