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Welllead Mesh Nebulizer Kit

EUDAMED

Class IIa (EU MDR)

Ref R01L013010Model Mesh Nebulizer Kit Basic

by Well Lead Medical Co., Ltd.

Identity

Trade Name
Welllead Mesh Nebulizer Kit EUDAMED
Device Name
Mesh Nebulizer Kit EUDAMED
Model / Reference
Mesh Nebulizer Kit Basic EUDAMED
R01L013010 EUDAMED

Identifiers

Primary DI / UDI-DI
06925816646195 EUDAMED
Basic UDI-DI
69449327FR01E00KF EUDAMED
EMDN Code
R03010304 AEROSOL THERAPY KITS EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

Yes

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

Welllead Mesh Nebulizer Kit by Well Lead Medical 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-000006728
Authorised Representative
Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001

Sources (1)

  • EUDAMED b98f7953-c3f3-4adc-8577-9f2cb9131c24 61 fields · synced Aug 3, 2026