Skip to content

Dr. Max PRO 32 x128 CZ/SK/PL/RO/RS/IT

by Helago-Pharma GmbH & Co. KG EUDAMED

Active European Union

Ref 900614Model Dr. Max PRO 32 x128 CZ/SK/PL/RO/RS/IT

Regulatory status

as of 27 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-34002033006148 Basic UDI-DIDate27 May 2026RegisteredStatusActive

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD Expiring

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

Model / Reference
Dr. Max PRO 32 x128 CZ/SK/PL/RO/RS/IT, 900614
Primary DI / UDI-DI
34002033006148
Basic UDI-DI
B-34002033006148
EMDN Code
D0599 Oxygen producers for disinfection of medical devices - other
Device Class
Class IIb
Market of Registration
Germany

Manufacturer details

EUDAMED SRN
DE-MF-000004933

Other devices from Helago-Pharma GmbH & Co. KG

See all devices from Helago-Pharma GmbH & Co. KG →

Properties

Other properties (11)

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