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26240

EUDAMED

Class IIa (EU MDR)

Ref 26240Model CURAMED CURA NEB KIT Ref 25715 - 25730Model CURAMED BENDA ORLATA

by Cura Farma Srl

Identity

Trade Name
CURAMED EUDAMED
Model / Reference
CURAMED CURA NEB KIT EUDAMED
26240 EUDAMED
CURAMED BENDA ORLATA EUDAMED
25715 - 25730 EUDAMED

Identifiers

Primary DI / UDI-DI
08055305950378 EUDAMED
08056590232514 EUDAMED
Basic UDI-DI
80553059503782J EUDAMED
80565902325143Y EUDAMED
EMDN Code
R03010380 AEROSOL THERAPY SYSTEMS - ACCESSORIES EUDAMED
M030101 HYDROPHILIC GAUZE BANDAGES EUDAMED

Classification

Device Class
Class IIa EUDAMED
Class I EUDAMED
Market of Registration
Italy EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMEDEUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

Yes

EUDAMEDEUDAMED

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

EUDAMEDEUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

26240 by Cura Farma Srl — 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
Cura Farma Srl
EUDAMED SRN
IT-MF-000011478

Sources (2)

  • EUDAMED 0316a4c0-dd94-49bb-82ae-f08e11cc87f3 61 fields · synced Aug 3, 2026
  • EUDAMED d605ef23-ea71-4460-82ed-d15b7ff86272 61 fields · synced May 18, 2026