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Molosil Plus Cartridge Only

FDA UDI

Class II (US FDA UDI)

by Protech Professional Products, Inc.

Identity

Trade Name
Molosil Plus Cartridge Only FDA UDI
Generic Name
Denture reliner, elastic, short-term FDA UDI
Device Name
Mollosil Plus 50 ml cartridge only FDA UDI
Model / Reference
FIXX2 FDA UDI
Description
Mollosil Plus 50 ml cartridge only FDA UDI

Identifiers

Primary DI / UDI-DI
D814FIXX21 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

Molosil Plus Cartridge Only 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 5a69f0e5-2b0e-4d6b-8ac9-a077516aa733 33 fields · synced Jun 8, 2026