Primary Device ID | EDD153654400022 |
NIH Device Record Key | 0f02f116-2120-4515-9b26-07c13f6a2160 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | CEREC |
Version Model Number | 5365440002 |
Catalog Number | 5365440002 |
Company DUNS | 329532225 |
Company Name | DeguDent GmbH |
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 | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
HIBCC | EDD153654400022 [Primary] |
EIH | POWDER, PORCELAIN |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-07-04 |
Device Publish Date | 2024-06-26 |
EDD153654400352 | 5365440035 |
EDD153654400322 | 5365440032 |
EDD153654400312 | 5365440031 |
EDD153654400282 | 5365440028 |
EDD153654400272 | 5365440027 |
EDD153654400252 | 5365440025 |
EDD153654400242 | 5365440024 |
EDD153654400232 | 5365440023 |
EDD153654400222 | 5365440022 |
EDD153654400212 | 5365440021 |
EDD153654400152 | 5365440015 |
EDD153654400122 | 5365440012 |
EDD153654400112 | 5365440011 |
EDD153654400082 | 5365440008 |
EDD153654400072 | 5365440007 |
EDD153654400052 | 5365440005 |
EDD153654400042 | 5365440004 |
EDD153654400032 | 5365440003 |
EDD153654400022 | 5365440002 |
EDD153654400012 | 5365440001 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() CEREC 79035119 3485105 Dead/Cancelled |
Dentsply Sirona, Inc 2006-05-05 |
![]() CEREC 73745477 1527765 Live/Registered |
BRANDESTINI, MARCO 1988-08-11 |