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SplintCushion

EUDAMED

Class I (EU MDR)

Ref NC12904-1BModel 826

by North Coast Medical Inc.

Identity

Trade Name
SplintCushion EUDAMED
Device Name
SplintCushion EUDAMED
Model / Reference
826 EUDAMED
NC12904-1B EUDAMED

Identifiers

Primary DI / UDI-DI
00768627007115 EUDAMED
Basic UDI-DI
0768627CSTACC-826-94 EUDAMED
Direct Marketing DI
00768627007115 EUDAMED
EMDN Code
M03030203 FOAM PADS EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Ireland 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

SplintCushion by North Coast Medical, Inc. — 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
US-MF-000009087
Authorised Representative
ICON (LR) Limited IE-AR-000006507

Sources (1)

  • EUDAMED a210eb6c-7c88-4ad3-ab17-52ebbd396a6b 61 fields · synced Jun 19, 2026