Primary Device ID | 08800000902753 |
NIH Device Record Key | c6470bc0-60e0-4bf5-99e7-9376a856efc3 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | US/SS/GS System |
Version Model Number | SSRA000D |
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 |