Primary Device ID | 08800000903781 |
NIH Device Record Key | 9bc54e38-c794-4fa7-9884-36f4744e12fb |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | US/SS/GS System |
Version Model Number | MEPW100TH |
Company DUNS | 689051793 |
Company Name | Osstem Implant Co., Ltd. |
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 | true |
Manufacturing Date | true |
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 |