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Gum Aftaclear Spray

EUDAMED

Class IIa (EU MDR)

Ref 2420FNLDIA

by Sunstar Europe SA

Identity

Trade Name
GUM AFTACLEAR SPRAY EUDAMED
Device Name
GUM AFTACLEAR SPRAY EUDAMED
Model / Reference
2420FNLDIA EUDAMED

Identifiers

Primary DI / UDI-DI
17630019900468 EUDAMED
Basic UDI-DI
B-17630019900468 EUDAMED
EMDN Code
M040499 DRESSINGS FOR WOUNDS, SORES AND ULCERATIONS - OTHER 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

Gum Aftaclear Spray by Sunstar Europe SA — 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
Sunstar Europe SA
EUDAMED SRN
CH-MF-000023162
Authorised Representative
Sunstar France FR-AR-000018318

Sources (1)

  • EUDAMED 64c8ec13-99f5-4fdf-8771-73d4d8700fef 61 fields · synced Jun 18, 2026