Skip to content

Dr. Max Spray per afte

by Global Pharma Cm S.a EUDAMED

Active European Union

Ref 131EN-2

Regulatory status

as of 26 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-131EN-24J Basic UDI-DIDate20 Aug 2024RegisteredStatusActive

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD Expiring

Certificates: none listed in EUDAMED

Specification

EUDAMED

Device Name
Spray do gardła
Model / Reference
131EN-2
Primary DI / UDI-DI
D-131EN-24J
Basic UDI-DI
B-131EN-24J
EMDN Code
Q030199 Nasopharyngeal devices - other
Device Class
Class I
Market of Registration
Italy

Manufacturer details

EUDAMED SRN
PL-MF-000034662

Other devices from Global Pharma Cm S.a

See all devices from Global Pharma Cm S.a →

Properties

Show 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