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MED-111 Compressor nebulizer

by B.Well Swiss AG EUDAMED

Active European Union

Ref 1101595Model MED-120, PRO-110, PRO-115, TH-130, MED-111, MED-130, PRO-100, PRO-101

Regulatory status

as of 28 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number764015639MDA0307_1M8 Basic UDI-DIDate8 Apr 2025RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Active

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Specification

EUDAMED

Device Name
Compressor nebulizer
Model / Reference
MED-120, PRO-110, PRO-115, TH-130, MED-111, MED-130, PRO-100, PRO-101, 1101595
Primary DI / UDI-DI
07640156398489
Basic UDI-DI
764015639MDA0307_1M8
Direct Marketing DI
07640156398489
EMDN Code
Z12159002 Aerosol equipment
Device Class
Class IIa
Market of Registration
Germany

Manufacturer details

EUDAMED SRN
CH-MF-000012588
Authorised representative
Blue Broccoli GmbH LI-AR-000000233

Other devices from B.Well Swiss AG

See all devices from B.Well Swiss AG →

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