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OMNI DENT Löffeladhäsiv Silikon Liquid

EUDAMED

Class I (EU MDR)

Ref 51293Model 122

by PRISMAN GmbH

Identity

Trade Name
OMNI DENT Löffeladhäsiv Silikon Liquid EUDAMED
Device Name
Adhäsiv Liquid SILICON EUDAMED
Model / Reference
122 EUDAMED
51293 EUDAMED

Identifiers

Primary DI / UDI-DI
04064797001073 EUDAMED
Basic UDI-DI
++EPRM122DF EUDAMED
EMDN Code
Q01020104 DENTAL IMPRESSION SILICONES EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Category: Silicone dental impression material

OMNI DENT Löffeladhäsiv Silikon Liquid by PRISMAN GmbH — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Silicone dental impression material.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

Manufacturer
PRISMAN GmbH
EUDAMED SRN
DE-MF-000009900

Sources (1)

  • EUDAMED 423d31fd-f402-4ffc-b6d0-d17d00572be1 61 fields · synced Jun 19, 2026