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Cavex ImpreSafe container

FDA UDI

Class I (US FDA UDI)

by Cavex Holland B.V.

Identity

Trade Name
Cavex ImpreSafe container FDA UDI
Generic Name
Denture cleanser FDA UDI
Device Name
Dental impression disinfectant FDA UDI
Model / Reference
HT020 FDA UDI
Description
Dental impression disinfectant FDA UDI

Identifiers

Catalog Number
HT020 FDA UDI
Primary DI / UDI-DI
E241HT0200 FDA UDI
FDA Product Code
LRJ FDA UDI
GMDN Term
Denture cleanser FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6890 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: Denture cleanser

Cavex ImpreSafe container by Cavex Holland B.V. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Denture cleanser.

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 48bad82a-5ec8-4df8-ba45-be2cac7135c2 36 fields · synced Jun 8, 2026