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Назопрес Спрей За Нос С Алое Вера И Пантенол

by Dr. Müller Pharma s.r.o.

Ref PC2101_015

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 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-08595610407162 Basic UDI-DI 08595610407162UDI-DIDate15 Jul 2025RegisteredStatusActive

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  • Withdrawn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
НАЗОПРЕС спрей за нос с алое вера и пантенол / NASOPRESS nasal spray with aloe vera and panthenol
Model / Reference
PC2101_015
Primary DI / UDI-DI
08595610407162
Basic UDI-DI
B-08595610407162
EMDN Code
Q030103 Nasal irrigation solutions
Device Class
Class I
EU market of registration
Bulgaria

Manufacturer details

EUDAMED SRN
CZ-MF-000000005

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

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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