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Miratray Implant OK S2

EUDAMED

Class I (EU MDR)

Ref 101252Model 000300

by Hager & Werken GmbH & Co. KG

Identity

Trade Name
Miratray Implant OK S2 EUDAMED
Device Name
Abformlöffel, für Implantate EUDAMED
Model / Reference
000300 EUDAMED
101252 EUDAMED

Identifiers

Primary DI / UDI-DI
04099637003061 EUDAMED
Basic UDI-DI
40996370003003D EUDAMED
Unit of Use DI
04099637003054 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

Category: Dental impression tray, single-use

Miratray Implant OK S2 by Hager & Werken GmbH & Co. KG — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Dental impression tray, single-use.

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 cae64757-251f-460d-8599-1aec053b6fe2 61 fields · synced Jun 17, 2026