Primary Device ID | 08809488215539 |
NIH Device Record Key | 16d1f70e-5dc5-43be-ba03-79463c9a74f0 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Two-Piece Type Abutments |
Version Model Number | TWA507020R |
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 |