Primary Device ID | 08806169098665 |
NIH Device Record Key | 1ea28f52-0f32-45b4-ab05-8063f57335e0 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | DIOnavi-Denture |
Version Model Number | 3DDEN-500 |
Catalog Number | 3DDEN-500 |
Company DUNS | 631085206 |
Company Name | DIO Corporation |
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 | false |
Lot Batch | true |
Serial Number | false |
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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 08806169098665 [Primary] |
EBI | Resin, Denture, Relining, Repairing, Rebasing |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2021-11-10 |
Device Publish Date | 2020-11-05 |
08806169098672 | DIOnavi-Denture is a light-curable resin indicated for fabrication and repair of full and partia |
08806169098665 | DIOnavi-Denture is a light-curable resin indicated for fabrication and repair of full and partia |
08806169098658 | DIOnavi-Denture is a light-curable resin indicated for fabrication and repair of full and partia |