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Nebulizer kit

EUDAMED

Class IIa (EU MDR)

Ref NK-101

by JOYTECH Healthcare Co., Ltd.

Identity

Trade Name
Nebulizer kit EUDAMED
Device Name
Nebulizer Kit EUDAMED
Model / Reference
NK-101 EUDAMED

Identifiers

Primary DI / UDI-DI
06942284617038 EUDAMED
Basic UDI-DI
6970392211NK00013D EUDAMED
EMDN Code
R03010304 AEROSOL THERAPY KITS EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Belgium 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

Yes

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Nebulizer kit by Joytech Healthcare Co., Ltd. — 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

EUDAMED SRN
CN-MF-000006020
Authorised Representative
Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001

Sources (1)

  • EUDAMED ea43d156-7007-480a-8d88-f944a21daa61 61 fields · synced Jun 18, 2026