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DTK adhesive opak

FDA UDI

Class I (US FDA UDI)

by bredent GmbH & Co. KG

Identity

Trade Name
DTK adhesive opak FDA UDI
Generic Name
Dental prosthesis priming agent FDA UDI
Device Name
DTK adhesive opak assortment in a double mixing cartridge 5 Parts FDA UDI
Model / Reference
54001285 FDA UDI
Description
DTK adhesive opak assortment in a double mixing cartridge 5 Parts FDA UDI

Identifiers

Catalog Number
54001285 FDA UDI
Primary DI / UDI-DI
EBRE540012850 FDA UDI
FDA Product Code
EGG FDA UDI
GMDN Term
Dental prosthesis priming agent FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.3165 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Dental prosthesis priming agent

DTK adhesive opak by bredent GmbH & Co. KG — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental prosthesis priming agent.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 094576d4-64e5-4887-ab24-aa0c32c8b381 35 fields · synced May 30, 2026