← Back to catalogue

Cavex Boil&Bite

FDA UDI

Class I (US FDA UDI)

by Cavex Holland B.V.

Identity

Trade Name
Cavex Boil&Bite FDA UDI
Generic Name
Dental bleaching agent FDA UDI
Device Name
Dental Whitening Agent FDA UDI
Model / Reference
BW085 FDA UDI
Description
Dental Whitening Agent FDA UDI

Identifiers

Catalog Number
BW085 FDA UDI
Primary DI / UDI-DI
E241BW0850 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 Boil&Bite 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Cavex Holland B.V.

Sources (1)

  • FDA UDI 9ec72517-e7fd-4fef-a620-89e346a44601 36 fields · synced May 30, 2026