Primary Device ID | 08800000902005 |
NIH Device Record Key | 3006fc71-7bb3-40f4-b5c7-d9f6d57e7e99 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | US/SS/GS System |
Version Model Number | GSTA5630NWH |
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 |