Primary Device ID | 10841307118527 |
NIH Device Record Key | df9b16af-e6da-4267-83e1-5abb1750dfeb |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Steri-Oss 3.8 - 4.0 Non-Hex Flat Top - Non-Hex Cylinder & .050"/1.25mm Hex Screw |
Version Model Number | 48-400252 |
Catalog Number | 48-400252 |
Company DUNS | 868856969 |
Company Name | IMPLANT DIRECT SYBRON MANUFACTURING LLC |
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 | true |
Device Combination Product | false |
Single Use | true |
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 |