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Exacta Evaluation Kit

EUDAMED

Class I (EU MDR)

Ref NC70142-HKModel 1656

by North Coast Medical Inc.

Identity

Trade Name
Exacta Evaluation Kit EUDAMED
Device Name
Exacta Evaluation Kit EUDAMED
Model / Reference
1656 EUDAMED
NC70142-HK EUDAMED

Identifiers

Primary DI / UDI-DI
00768627004770 EUDAMED
Basic UDI-DI
0768627REHAB-1656-SK EUDAMED
Direct Marketing DI
00768627004770 EUDAMED
EMDN Code
Z12069099 VARIOUS PHYSIOTHERAPY AND REHABILITATION INSTRUMENTS - OTHER EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Austria 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

Exacta Evaluation 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 7edf7074-7e02-4293-a630-1d8cd0b52577 61 fields · synced Jun 18, 2026