Primary Device ID | 08809488214594 |
NIH Device Record Key | d0489143-0b31-4748-a97b-78173d63e6dc |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | One-Piece Type Abutments |
Version Model Number | OPA404030R |
Company DUNS | 688476027 |
Company Name | KJMEDITECH.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 | false |
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 |