Primary Device ID | 00889024343955 |
NIH Device Record Key | c631bd57-2695-4667-8c39-0819a8c6e73f |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Eztetic |
Version Model Number | CX20A3 |
Company DUNS | 103167086 |
Company Name | ZIMMER DENTAL INC. |
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 | false |
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 | 00889024343955 [Primary] |
DZE | IMPLANT, ENDOSSEOUS, ROOT-FORM |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 5 |
Public Version Date | 2019-11-08 |
Device Publish Date | 2016-05-24 |
00889024344457 | CNEANP31 |
00889024343955 | CX20A3 |
00889024343917 | CT318 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
EZTETIC 86421929 5218886 Live/Registered |
Zimmer Dental Inc. 2014-10-13 |