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Guide

EUDAMED

Class I (EU MDR)

Ref C0021

by ORTHOTECH Co., Ltd

Identity

Trade Name
Guide EUDAMED
Device Name
Orthopaedic Instrument EUDAMED
Model / Reference
C0021 EUDAMED

Identifiers

Primary DI / UDI-DI
08800045323490 EUDAMED
Basic UDI-DI
88000453BEOTI001KA EUDAMED
EMDN Code
L091199 ORTHOPAEDIC PROSTHETICS INSTRUMENTS, REUSABLE - OTHER 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

Guide by ORTHOTECH Co., Ltd — 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

Manufacturer
ORTHOTECH Co., Ltd
EUDAMED SRN
KR-MF-000048890
Authorised Representative
AF Pharma Service Europe SL ES-AR-000018076

Sources (1)

  • EUDAMED f8fbc77a-e68e-4de9-a0a6-9f0e588372e3 61 fields · synced Jun 19, 2026