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Splint

EUDAMED

Class I (EU MDR)

Ref DW-FS03-F-15

by Suzhou Ireland Medical Equipment Co., Ltd.

Identity

Trade Name
Splint EUDAMED
Device Name
Splint EUDAMED
Model / Reference
DW-FS03-F-15 EUDAMED

Identifiers

Primary DI / UDI-DI
06977728545486 EUDAMED
Basic UDI-DI
697772854DWSPXE EUDAMED
Direct Marketing DI
06977728545486 EUDAMED
EMDN Code
M03050299 BANDAGES AND SPLINTS - 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

Category: Hand/finger splint, reusable

Splint by Suzhou Ireland Medical Equipment Co., Ltd. — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Hand/finger splint, reusable.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
CN-MF-000043757
Authorised Representative
MedPath GmbH DE-AR-000000087

Sources (1)

  • EUDAMED 86a476a1-eb38-47bc-835f-af82b7d95b5f 61 fields · synced Jun 19, 2026