Primary Device ID | 07615208479058 |
NIH Device Record Key | 69bedb93-3427-4eb6-a47c-59e9b8fadf00 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | IPS e.max ZirCAD |
Version Model Number | 725180 |
Catalog Number | 725180 |
Company DUNS | 448015938 |
Company Name | IVOCLAR VIVADENT AKTIENGESELLSCHAFT |
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 | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 07615208479058 [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 | 2024-02-29 |
Device Publish Date | 2024-02-21 |
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Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() IPS E.MAX ZIRCAD 77396632 3629541 Live/Registered |
Ivoclar Vivadent, Inc. 2008-02-14 |