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Caps Warmer

FDA UDI

Class I (US FDA UDI)

by VOCO GmbH

Identity

Trade Name
Caps Warmer FDA UDI
Generic Name
Anaesthesia warmer FDA UDI
Device Name
Device for temporary heating of dental composites in order to improve application properties. FDA UDI
Model / Reference
9002 FDA UDI
Description
Device for temporary heating of dental composites in order to improve application properties. FDA UDI

Identifiers

Primary DI / UDI-DI
E22190021 FDA UDI
FDA Product Code
EFC FDA UDI
EEG FDA UDI
EBZ FDA UDI
GMDN Term
Anaesthesia warmer FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.6100 FDA UDI
872.6475 FDA UDI
872.6070 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

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Anaesthesia warmer

Caps Warmer by VOCO GmbH — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Anaesthesia warmer.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
VOCO GmbH

Sources (1)

  • FDA UDI 398b4b8a-556b-4fc5-a618-db08c7fa0c3e 34 fields · synced May 30, 2026