← Back to catalogue

Gum Aftaclear Gel

EUDAMED

Class IIa (EU MDR)

Ref 2400FNLDA

by Sunstar Europe SA

Identity

Trade Name
GUM AFTACLEAR GEL EUDAMED
Device Name
GUM AFTACLEAR GEL EUDAMED
Model / Reference
2400FNLDA EUDAMED

Identifiers

Primary DI / UDI-DI
17630019900253 EUDAMED
Basic UDI-DI
B-17630019900253 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

Category: Negative-pressure wound therapy system foam dressing, non-antimicrobial

Gum Aftaclear Gel by Sunstar Europe SA — Class IIa — MDD — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Negative-pressure wound therapy system foam dressing, non-antimicrobial.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Sunstar Europe SA
EUDAMED SRN
CH-MF-000023162
Authorised Representative
Sunstar France FR-AR-000018318

Sources (1)

  • EUDAMED f915de94-0c46-49bd-9a23-2242caba8f45 61 fields · synced Jun 18, 2026