Primary Device ID | 08800209320303 |
NIH Device Record Key | c6a76ec3-d5ea-4e15-a40d-dd7d628908e7 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | SS SA Fixture System |
Version Model Number | SS3R3508S18 |
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 | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |