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Diamond

FDA UDI

Class I (US FDA UDI)

by Dentscare Ltda

Identity

Trade Name
Diamond FDA UDI
Generic Name
Dentifrice FDA UDI
Device Name
Polishing paste based on aluminum oxide with extra fine grit (6 to 8 microns), soluble in water, used to meet the requirements of polishing and shine of resins in general. FDA UDI
Model / Reference
R FDA UDI
Description
Polishing paste based on aluminum oxide with extra fine grit (6 to 8 microns), soluble in water, used to meet the requirements of polishing and shine of resins in general. FDA UDI

Identifiers

Catalog Number
4000002092 FDA UDI
Primary DI / UDI-DI
07898032320127 FDA UDI
FDA Product Code
EJR FDA UDI
GMDN Term
Dentifrice FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.6030 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Dentifrice

Diamond by Dentscare Ltda — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dentifrice.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Dentscare Ltda

Sources (1)

  • FDA UDI 32756196-5559-4f2b-bcab-73583987b081 34 fields · synced Jun 8, 2026