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Percutaneous Arm

EUDAMED

Class I (EU MDR)

Ref 1506200200

by Changzhou Waston Medical Appliance Co., Ltd

Identity

Trade Name
Percutaneous Arm EUDAMED
Device Name
Percutaneous Arm EUDAMED
Model / Reference
1506200200 EUDAMED

Identifiers

Primary DI / UDI-DI
06941317452936 EUDAMED
Basic UDI-DI
B-06941317452936 EUDAMED
EMDN Code
L0922 ORTHOPAEDIC SURGERY GUIDES, REUSABLE EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Netherlands EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

Yes

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

Percutaneous Arm by Changzhou Waston Medical Appliance Co., Ltd — Class I — MDD — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

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Manufacturer

EUDAMED SRN
CN-MF-000004851
Authorised Representative
Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001

Sources (1)

  • EUDAMED da7ece66-1aea-4a36-872e-76c0d2373398 61 fields · synced Sep 17, 2026