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Freeprint denture 385 500g

FDA UDI

Class II (US FDA UDI)

by DETAX GmbH & Co. KG

Identity

Trade Name
Freeprint denture 385 500g FDA UDI
Generic Name
Denture reliner, elastic, long-term FDA UDI
Model / Reference
02133 FDA UDI

Identifiers

Primary DI / UDI-DI
EDET021331 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

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, long-term

Freeprint denture 385 500g by DETAX GmbH & Co. KG — 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

Manufacturer
DETAX GmbH & Co. KG

Sources (1)

  • FDA UDI 43c2f526-1b76-4f50-859f-013cd2d6e37e 33 fields · synced May 30, 2026