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Ufi Gel hard C

FDA UDI

Class II (US FDA UDI)

by VOCO GmbH

Identity

Trade Name
Ufi Gel hard C FDA UDI
Generic Name
Denture reliner, hard FDA UDI
Device Name
Hard direct denture relining. The kit contains set cartridge 80 g, adhesive bottle 10 ml and accessories. FDA UDI
Model / Reference
2215 FDA UDI
Description
Hard direct denture relining. The kit contains set cartridge 80 g, adhesive bottle 10 ml and accessories. FDA UDI

Identifiers

Catalog Number
2215 FDA UDI
Primary DI / UDI-DI
E22122151 FDA UDI
FDA Product Code
EBI FDA UDI
GMDN Term
Denture reliner, hard FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3760 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

Yes

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Denture reliner, hard

Ufi Gel hard C by VOCO GmbH — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Denture reliner, hard.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
VOCO GmbH

Sources (1)

  • FDA UDI e88c4b44-86e8-4df5-91fd-d392e2a181ce 36 fields · synced Jun 6, 2026