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Splint

EUDAMED

Class I (EU MDR)

Ref FS-231LC

by FIRSTAR HEALTHCARE COMPANY LlMITED(GUANGZHOU)

Identity

Trade Name
SPLINT EUDAMED
Device Name
MEDICAL SPLINT EUDAMED
Model / Reference
FS-231LC EUDAMED

Identifiers

Primary DI / UDI-DI
06942272682314 EUDAMED
Basic UDI-DI
69422726P4.02.01XL EUDAMED
EMDN Code
M03050202 SYNTHETIC CAST BANDAGES AND SPLINTS 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

Splint by FIRSTAR HEALTHCARE COMPANY LlMITED(GUANGZHOU) — 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-000009645
Authorised Representative
MedPath GmbH DE-AR-000000087

Sources (1)

  • EUDAMED 3ee1e3f7-d572-4f63-8039-5ad787d66d7f 61 fields · synced Oct 7, 2026