Primary Device ID | DIVO5970561 |
NIH Device Record Key | 87b93f33-0ec0-4e57-83ad-4d499450ed5d |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Modeling Liquids Ceramic |
Version Model Number | 597056 |
Catalog Number | 597056 |
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 | 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 |
---|---|
HIBCC | DIVO5970561 [Primary] |
EIH | POWDER, PORCELAIN |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2020-05-13 |
Device Publish Date | 2016-11-09 |
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