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Miratray OK S1 12er

EUDAMED

Class I (EU MDR)

Ref 101170Model 000200

by Hager & Werken GmbH & Co. KG

Identity

Trade Name
Miratray OK S1 12er EUDAMED
Device Name
Abformlöffel, einmalige Anwendung EUDAMED
Model / Reference
000200 EUDAMED
101170 EUDAMED

Identifiers

Primary DI / UDI-DI
04099637002842 EUDAMED
Basic UDI-DI
409963700020038 EUDAMED
Unit of Use DI
04099637002835 EUDAMED
EMDN Code
Q010503 IMPRESSION MATERIAL TRAYS, SINGLE-USE 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

Miratray OK S1 12er by Hager & Werken GmbH & Co. KG — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
DE-MF-000004938

Sources (1)

  • EUDAMED b66a6641-d698-4fcc-8daa-21eb4ba3d420 61 fields · synced Oct 6, 2026