PROPHY PASTE

GUDID D89260705405712

MAXILL, INC.

Dentifrice
Primary Device IDD89260705405712
NIH Device Record Keyeaa30663-bf6f-47f3-bc70-c9b70f660b9c
Commercial Distribution StatusIn Commercial Distribution
Brand NamePROPHY PASTE
Version Model Number6070540571
Company DUNS079343581
Company NameMAXILL, INC.
Device Count200
DM Exemptfalse
Pre-market Exempttrue
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchfalse
Serial Numberfalse
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
HIBCCD89260705405710 [Unit of Use]
HIBCCD89260705405711 [Primary]
HIBCCD89260705405712 [Package]
Contains: D89260705405711
Package: Case [4000 Units]
In Commercial Distribution

FDA Product Code

EJRAgent, Polishing, Abrasive, Oral Cavity

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2022-10-28
Device Publish Date2022-10-20

On-Brand Devices [PROPHY PASTE]

D892607054058526070540585
D892607054058126070540581
D892607054057626070540576
D892607054057526070540575
D892607054057226070540572
D892607054057126070540571
D892607054056626070540566
D892607054056526070540565
D892607054056226070540562
D892607054056126070540561
D892607054056026070540560
D892607054055026070540550

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