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KaVo PROPHYpearls mint

FDA UDI

Class I (US FDA UDI)

by KaVo Dental GmbH

Identity

Trade Name
KaVo PROPHYpearls mint FDA UDI
Generic Name
Dentifrice FDA UDI
Model / Reference
1.010.1828 FDA UDI

Identifiers

Catalog Number
mint FDA UDI
Primary DI / UDI-DI
EKAV101018280 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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Dentifrice

KaVo PROPHYpearls mint by KaVo Dental GmbH — 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
KaVo Dental GmbH

Sources (1)

  • FDA UDI 41f1f342-d461-4658-b7c9-d4ac071e22ad 35 fields · synced May 30, 2026