← Back to catalogue

Spectra Q+

EUDAMED

Class IIa (EU MDR)

Ref NAModel Spectra Q+

by Uzinmedicare

Identity

Trade Name
SPECTRA Q+ EUDAMED
SPECTRA Q EUDAMED
Device Name
Electric breast pump EUDAMED
Model / Reference
Spectra Q+ EUDAMED
NA EUDAMED

Identifiers

Primary DI / UDI-DI
08809108018342 EUDAMED
08809108018267 EUDAMED
08809108018359 EUDAMED
Basic UDI-DI
880910801SPQP001TH EUDAMED
Direct Marketing DI
08809108018342 EUDAMED
08809108018267 EUDAMED
08809108018359 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 Q+ 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Uzinmedicare
EUDAMED SRN
KR-MF-000031282
Authorised Representative
Obelis s.a. BE-AR-000000106

Sources (3)

  • EUDAMED cf96e072-6e61-4af6-8fd9-72ce5bde72fc 61 fields · synced Jul 23, 2026
  • EUDAMED 240e3af9-49cf-4e93-9023-417fc5691aef 61 fields · synced May 19, 2026
  • EUDAMED 2f3d96d2-da46-41a3-a605-634cc10c07ba 61 fields · synced May 19, 2026