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Glicerino žvakutės 2, 2 g Dr. Müller Pharma

by Dr. Müller Pharma s.r.o.

Ref PC8801_014

Active European Union

CE MDD

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None, self-declared

Class I: no certifier involved

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-08595610407391 Basic UDI-DI 08595610407391UDI-DIDate9 Apr 2026RegisteredStatusActive

Certificates

0 certificates · EUDAMED

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

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD Active

Specification

EUDAMED

Device Name
Glicerino žvakutės 2,2 g Dr. Müller Pharma/Glicerīna svecītes 2,2 g Dr. Müller Pharma/Glütseriini suposiidid 2,2 g Dr. Müller Pharma
Model / Reference
PC8801_014
Primary DI / UDI-DI
08595610407391
Basic UDI-DI
B-08595610407391
EMDN Code
G05 Topical anorectal administered gastro-intestinal system devices
Device Class
Class I
EU market of registration
Lithuania

Manufacturer details

EUDAMED SRN
CZ-MF-000000005

Other devices from Dr. Müller Pharma s.r.o.

See all devices from Dr. Müller Pharma s.r.o. →

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