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Remescar

EUDAMED

Class IIa (EU MDR)

Ref 50 ml

by Sylphar nv

Identity

Trade Name
Remescar EUDAMED
Device Name
Remescar Spider Veins EUDAMED
Model / Reference
50 ml EUDAMED

Identifiers

Primary DI / UDI-DI
05425012531154 EUDAMED
Basic UDI-DI
B-05425012531154 EUDAMED
EMDN Code
M9002 PROTECTIVE DEVICES, LUBRICANTS AND SOOTHING DEVICES (SPRAYS, GELS, FLUIDS AND CREAMS) EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Spain EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Remescar by Sylphar nv — Class IIa — MDD — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

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Manufacturer

Manufacturer
Sylphar nv
EUDAMED SRN
BE-MF-000000732

Sources (1)

  • EUDAMED a6230255-9c13-42e7-a0dd-cc5b81e109b4 61 fields · synced Jun 19, 2026