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Cavex Bite&White patient kit

FDA UDI

Class I (US FDA UDI)

by Cavex Holland B.V.

Identity

Trade Name
Cavex Bite&White patient kit FDA UDI
Generic Name
Dental bleaching agent FDA UDI
Device Name
Dental Whitening Agent FDA UDI
Model / Reference
BW000 FDA UDI
Description
Dental Whitening Agent FDA UDI

Identifiers

Catalog Number
BW000 FDA UDI
Primary DI / UDI-DI
E241BW0000 FDA UDI
FDA Product Code
EEG FDA UDI
GMDN Term
Dental bleaching agent FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.6475 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

No

FDA UDI

Over-the-Counter

Yes

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

No

FDA UDI
MRI Safety
MR Safe FDA UDI

Category: Dental bleaching agent

Cavex Bite&White patient kit by Cavex Holland B.V. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental bleaching agent.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Cavex Holland B.V.

Sources (1)

  • FDA UDI 9970db5e-4595-4d36-a48c-e120aab6430e 37 fields · synced May 30, 2026