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Mollosil Plus Glaze and Catalyst

FDA UDI

Class II (US FDA UDI)

by Protech Professional Products, Inc.

Identity

Trade Name
Mollosil Plus Glaze and Catalyst FDA UDI
Generic Name
Denture reliner, elastic, short-term FDA UDI
Device Name
Mollosil Plue Glaze and Catalyst (2x7ml), Silicone Glaze and Catalyst and Nipples FDA UDI
Model / Reference
FIXX4 FDA UDI
Description
Mollosil Plue Glaze and Catalyst (2x7ml), Silicone Glaze and Catalyst and Nipples FDA UDI

Identifiers

Primary DI / UDI-DI
D814FIXX41 FDA UDI
FDA Product Code
EBI FDA UDI
GMDN Term
Denture reliner, elastic, short-term 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

No

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Denture reliner, elastic, short-term

Mollosil Plus Glaze and Catalyst by Protech Professional Products, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Denture reliner, elastic, short-term.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI db970d24-5d37-47ce-8f20-3c47ca80e930 33 fields · synced Jun 1, 2026