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Non Sterile-Silicone Nasal Splints

by Medasil Surgical Limited EUDAMED

Active European Union

Ref 120-1020-3257

Regulatory status

as of 26 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number506046556120-10AK Basic UDI-DIDate12 Mar 2025RegisteredStatusActive

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Certificates: none listed in EUDAMED

Specification

EUDAMED

Device Name
Non Sterile-Silicone Nasal Splints
Model / Reference
120-1020-3257
Primary DI / UDI-DI
05060465560391
Basic UDI-DI
506046556120-10AK
EMDN Code
P020203 Nasal splints
Device Class
Class IIa
Market of Registration
Ireland

Manufacturer details

EUDAMED SRN
GB-MF-000009549
Authorised representative
European Healthcare & Device Solutions Ltd. IE-AR-000003999

Related devices

Category: External nasal splint

Other devices from Medasil Surgical Limited

See all devices from Medasil Surgical Limited →

Properties

Show properties
  • Incorporates Medicinal Product
Other properties (12)
  • 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