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Sony

EUDAMED

Class I (EU MDR)

Ref NUA-BK30

by Sony Corporation

Identity

Trade Name
SONY EUDAMED
Device Name
IP Converter Bracket EUDAMED
Model / Reference
NUA-BK30 EUDAMED

Identifiers

Primary DI / UDI-DI
04548736105485 EUDAMED
Basic UDI-DI
4901780MonitorACC36J EUDAMED
EMDN Code
V9099 VARIOUS DEVICES NOT INCLUDED IN OTHER CLASSES - OTHER EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Netherlands 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

Category: Device sterilization/disinfection container, reusable

Sony by Sony Corporation — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Device sterilization/disinfection container, reusable.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

Manufacturer
Sony Corporation
EUDAMED SRN
JP-MF-000014553
Authorised Representative
Sony Belgium, bijkantoor van Sony Europe B.V. BE-AR-000007876

Sources (1)

  • EUDAMED b67128b2-d0d0-4f67-a49c-b3f2cc8c704d 61 fields · synced May 22, 2026