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Remescar

by Sylphar nv 4 variants

Ref 50 ml

Remescar (50 ml) is a medical device (EU MDD Class IIa; EMDN category protective devices) made by Sylphar nv, registered in EUDAMED on 29 Oct 2021 (Basic UDI-DI B-05425012531154), active as of 24 Oct 2026.

Active European Union

CE MDD

Valid until

No date given

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Source EUDAMED, synced 24 Oct 2026.

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-05425012531154 Basic UDI-DI 05425012531154UDI-DIDate29 Oct 2021RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD Active

Specification

EUDAMED

Device name
Remescar Spider Veins
Model / reference
50 ml
Primary DI / UDI-DI
05425012531154
Basic UDI-DI
B-05425012531154
EMDN code
M9002 Protective devices, lubricants and soothing devices (sprays, gels, fluids and creams)
Device class
Class IIa
EU registration type
Legacy device (under a directive)
EU market of registration
Spain

Manufacturer details

EUDAMED SRN
BE-MF-000000732

Similar devices in this category

Other devices filed under PROTECTIVE DEVICES, LUBRICANTS AND SOOTHING DEVICES (SPRAYS, GELS, FLUIDS AND CREAMS).

Other devices from Sylphar nv

See all devices from Sylphar nv →

Properties

Other properties (12, all answered No)