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Gum Hydral Mouthrinse

EUDAMED

Class I (EU MDR)

Ref 6030

by Sunstar Europe SA

Identity

Trade Name
GUM HYDRAL MOUTHRINSE EUDAMED
Device Name
GUM HYDRAL MOUTHRINSE EUDAMED
Model / Reference
6030 EUDAMED

Identifiers

Primary DI / UDI-DI
17630019900628 EUDAMED
Basic UDI-DI
B-17630019900628 EUDAMED
EMDN Code
V9099 VARIOUS DEVICES NOT INCLUDED IN OTHER CLASSES - OTHER EUDAMED

Classification

Device Class
Class I 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: Device sterilization/disinfection container, reusable

Gum Hydral Mouthrinse by Sunstar Europe SA — Class I — MDD — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Device sterilization/disinfection container, reusable.

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 1efabc32-0812-45d2-83d7-4d396c70f533 61 fields · synced Oct 6, 2026