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Spectra 9Plus

EUDAMED

Class IIa (EU MDR)

Ref NAModel Spectra 9Plus

by Uzinmedicare

Identity

Trade Name
Spectra 9Plus EUDAMED
Device Name
Electric breast pump EUDAMED
Model / Reference
Spectra 9Plus EUDAMED
NA EUDAMED

Identifiers

Primary DI / UDI-DI
08809108018229 EUDAMED
Basic UDI-DI
880910801SP9P001KL EUDAMED
Direct Marketing DI
08809108018229 EUDAMED
EMDN Code
Z12080303 BREAST PUMPS EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
France 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

Spectra 9Plus by Uzinmedicare — 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
Uzinmedicare
EUDAMED SRN
KR-MF-000031282
Authorised Representative
Obelis s.a. BE-AR-000000106

Sources (1)

  • EUDAMED ece65774-6403-484a-a9d6-b3fde910bf1e 61 fields · synced Jun 18, 2026