Primary Device ID | E27665742500 |
NIH Device Record Key | 1248b987-40cf-4e20-9286-746b2088ca53 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | CEREC SW |
Version Model Number | 6574250 |
Company DUNS | 340306351 |
Company Name | SIRONA Dental Systems 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 | false |
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 |
Device Issuing Agency | Device ID |
---|---|
HIBCC | E27665742500 [Primary] |
NHA | Abutment, Implant, Dental, Endosseous |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2016-09-10 |
E27665802650 | CEREC SW 4.4.1 |
E27665742500 | CEREC Premium CAM SW 4.4.0 |
E27665621070 | CEREC Ortho SW 1.1 |
E27665538820 | inLab CAM 15.0 |
E27665538740 | inLab SW 15.0 |
E27665530310 | CEREC Premium SW 4.4.0 |
E27665530230 | CEREC SW 4.4 |