Maxigold 582054

GUDID D7075820540

Maxigold 5 g

IVOCLAR VIVADENT, INC.

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Primary Device IDD7075820540
NIH Device Record Keyc4e38751-e8af-4762-8297-414c0496057c
Commercial Distribution StatusIn Commercial Distribution
Brand NameMaxigold
Version Model Number582054
Catalog Number582054
Company DUNS176935203
Company NameIVOCLAR VIVADENT, INC.
Device Count1
DM Exemptfalse
Pre-market Exempttrue
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchtrue
Serial Numberfalse
Manufacturing Datetrue
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
HIBCCD7075820540 [Primary]

FDA Product Code

EJTAlloy, gold-based noble metal

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2022-04-27
Device Publish Date2018-10-29

On-Brand Devices [Maxigold]

D7075766300Maxigold 100 g
D7075766290Maxigold 25 g
D7075820560Maxigold 1oz/31 g
D7075820540Maxigold 5 g

Trademark Results [Maxigold]

Mark Image

Registration | Serial
Company
Trademark
Application Date
MAXIGOLD
MAXIGOLD
73087583 1056429 Live/Registered
WILLIAMS GOLD REFINING COMPANY INCORPORATED
1976-05-18

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