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Base 2 Single Finger Extension Kit

EUDAMED

Class I (EU MDR)

Ref NC12820Model 681

by North Coast Medical Inc.

Identity

Trade Name
Base 2 Single Finger Extension Kit EUDAMED
Device Name
Base 2 Single Finger Extension Kit EUDAMED
Model / Reference
681 EUDAMED
NC12820 EUDAMED

Identifiers

Primary DI / UDI-DI
00768627015295 EUDAMED
Basic UDI-DI
0768627CSTACC-681-95 EUDAMED
Direct Marketing DI
00768627015295 EUDAMED
EMDN Code
M030504 IMMOBILISATION SYSTEMS, MOULDABLE UNDER COLD AND HOT TEMPERATURES EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Sweden 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

Base 2 Single Finger Extension Kit 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 73ed9621-fa1a-4749-8d20-57abb9caa90e 61 fields · synced Jun 18, 2026