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Sofreliner Tough

FDA UDI

Class II (US FDA UDI)

by Tokuyama Dental Corporation

Identity

Trade Name
Sofreliner Tough FDA UDI
Generic Name
Denture reliner, elastic, long-term FDA UDI
Device Name
S Paste FDA UDI
Model / Reference
23411 FDA UDI
Description
S Paste FDA UDI

Identifiers

Primary DI / UDI-DI
04548190234110 FDA UDI
FDA Product Code
EBI FDA UDI
GMDN Term
Denture reliner, elastic, long-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

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Denture reliner, elastic, short-termDenture reliner, elastic, long-term

Sofreliner Tough by Tokuyama Dental Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

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

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 62d5661b-a557-46ef-ad07-f6bd98e984b6 35 fields · synced May 30, 2026