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RF1 Nebulizer w/Valve T Kit, 22F, 22M

EUDAMED

Class IIa (EU MDR)

Ref AD0005Model (E) Aerosol Therapy

by GaleMed Corporation

Identity

Trade Name
RF1 Nebulizer w/Valve T Kit, 22F, 22M EUDAMED
Device Name
Nebulizer Kit EUDAMED
Model / Reference
(E) Aerosol Therapy EUDAMED
AD0005 EUDAMED

Identifiers

Primary DI / UDI-DI
04710810100543 EUDAMED
Basic UDI-DI
471081008NNED8B EUDAMED
EMDN Code
R03010304 AEROSOL THERAPY KITS EUDAMED

Classification

Device Class
Class IIa 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

RF1 Nebulizer w/Valve T Kit, 22F, 22M by GaleMed Corporation — 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
GaleMed Corporation
EUDAMED SRN
TW-MF-000022411
Authorised Representative
Emergo Europe B.V. NL-AR-000000116

Sources (1)

  • EUDAMED ae03ce74-c5c3-4ef9-b0c7-4a0c945f671e 61 fields · synced Jun 17, 2026