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Reusable, Non-Sterile, Instrument Case

EUDAMED

Class I (EU MDR)

Ref 23500002

by Shandong Weigao Orthopaedic Device Company Limited.

Identity

Device Name
Reusable, Non-Sterile, Instrument Case EUDAMED
Model / Reference
23500002 EUDAMED

Identifiers

Primary DI / UDI-DI
06942420064047 EUDAMED
Basic UDI-DI
6903095SCAS07V6 EUDAMED
EMDN Code
L0919 ORTHOPAEDIC AND TRAUMATOLOGICAL SURGERY INSTRUMENT KITS, REUSABLE EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Germany 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

Reusable, Non-Sterile, Instrument Case by Shandong Weigao Orthopaedic Device Company Limited. — 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
CN-MF-000019785
Authorised Representative
Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001

Sources (1)

  • EUDAMED ee929701-e837-4479-a9a2-818a0cbd65de 61 fields · synced Jun 19, 2026