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Duk-In Splint

EUDAMED

Class I (EU MDR)

Ref S3855Model Splint

by Duk-In Co., Ltd.

Identity

Trade Name
Duk-In Splint EUDAMED
Device Name
Synthetic Orthopedic Splint EUDAMED
Model / Reference
Splint EUDAMED
S3855 EUDAMED

Identifiers

Primary DI / UDI-DI
08800033701422 EUDAMED
Basic UDI-DI
88000337SP100FF EUDAMED
Direct Marketing DI
08800033701422 EUDAMED
EMDN Code
M03050202 SYNTHETIC CAST BANDAGES AND SPLINTS EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Malta 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: Cotton wool roll, sterile

Duk-In Splint by Duk-In Co., Ltd. — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Cotton wool roll, sterile.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

Manufacturer
Duk-In Co., Ltd.
EUDAMED SRN
KR-MF-000026961
Authorised Representative
CMC Medical Devices & Drugs SL ES-AR-000000293

Sources (1)

  • EUDAMED 7faf5653-26d6-40bb-a8e8-8d9223655e0f 61 fields · synced Jul 9, 2026