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PEMF Blu

by B.A.C. Srl EUDAMED

Active European Union

Ref 11.0033.1.01Model PEMF Giallo, PEMF Giallo+, PEMF Bianco, PEMF Bianco+, PEMF Blu, PEMF Blu+, PEMF Marrone, PEMF Marrone+

Regulatory status

as of 27 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number805050389PEMFBK Basic UDI-DIDate21 Oct 2025RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not known
  • Not covered

European Union — CE/MDR Active

Certificates

0 certificates · EUDAMED

No notified-body certificate is listed. Devices of this class are self-declared by the manufacturer.

Specification

EUDAMED

Device Name
pemf
Model / Reference
PEMF Giallo, PEMF Giallo+, PEMF Bianco, PEMF Bianco+, PEMF Blu, PEMF Blu+, PEMF Marrone, PEMF Marrone+, 11.0033.1.01
Primary DI / UDI-DI
08050503890006
Basic UDI-DI
805050389PEMFBK
EMDN Code
Z120606 Magnetotherapy equipment
Device Class
Class I
Market of Registration
Italy

Manufacturer details

EUDAMED SRN
IT-MF-000013508

Properties

Other properties (13)

  • Sterile: No
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No