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C1054002

EUDAMED

Class IIa (EU MDR)

Ref C1054002Model MDA0000034

by Nakanishi Inc.

Identity

Model / Reference
MDA0000034 EUDAMED
C1054002 EUDAMED

Identifiers

Primary DI / UDI-DI
04560264529656 EUDAMED
Basic UDI-DI
456022498000003472 EUDAMED
Direct Marketing DI
04560264578494 EUDAMED
EMDN Code
Z12119007 DENTAL PROPHYLAXIS EQUIPMENT EUDAMED

Classification

Device Class
Class IIa 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

Yes

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

C1054002 by Nakanishi Inc. — Class IIa — 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

Manufacturer
Nakanishi Inc.
EUDAMED SRN
JP-MF-000011271
Authorised Representative
NSK Europe GmbH DE-AR-000007040

Sources (1)

  • EUDAMED 5bd3ab8f-0545-4396-97c1-361c2f9f8cbd 61 fields · synced Jun 18, 2026