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Neb Pro

EUDAMED

Class IIa (EU MDR)

Ref p957010-1

by Globalcare Medical Technology Co., Ltd.

Identity

Trade Name
NEB PRO EUDAMED
Device Name
Aerosoltherapy Nebulizer EUDAMED
Model / Reference
p957010-1 EUDAMED

Identifiers

Primary DI / UDI-DI
06970229253393 EUDAMED
Basic UDI-DI
697022925GCE8XXEM EUDAMED
EMDN Code
Z12159002 AEROSOL EQUIPMENT EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Lithuania 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

Neb Pro by Globalcare Medical Technology 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-000033595
Authorised Representative
Donawa Lifescience Consulting Srl IT-AR-000007785

Sources (1)

  • EUDAMED d8a3b23d-77ab-4ae1-bc53-7df4912b081e 61 fields · synced Jun 18, 2026