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Ea1203x050

EUDAMED

Class IIa (EU MDR)

Ref EA1203X050Model MDA0000219

by Nakanishi Inc.

Identity

Model / Reference
MDA0000219 EUDAMED
EA1203X050 EUDAMED

Identifiers

Primary DI / UDI-DI
04589551392384 EUDAMED
Basic UDI-DI
45602249800002197G EUDAMED
Direct Marketing DI
04560264577763 EUDAMED
EMDN Code
Z12119001 TARTAR ABLATORS 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

Ea1203x050 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 70e2081e-f168-4357-917f-3555dcbfe3d2 61 fields · synced Jul 13, 2026