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HAderm

EUDAMED

Class III (EU MDR)

Ref 01-02-07Model Derm (2.0ml, HAderm®)

by Shanghai Reyoungel Medical Technology Company Limited

Identity

Trade Name
HAderm EUDAMED
Device Name
Medical Cross-linked Sodium Hyaluronate Gel-Soft Tissue Filler EUDAMED
Model / Reference
Derm (2.0ml, HAderm®) EUDAMED
01-02-07 EUDAMED

Identifiers

Primary DI / UDI-DI
06974656020375 EUDAMED
Basic UDI-DI
B-06974656020375 EUDAMED
EMDN Code
P900402 RESORBABLE FILLING AND RECONSTRUCTION DEVICES EUDAMED

Classification

Device Class
Class III EUDAMED
Market of Registration
Poland EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMED

Implantable

Yes

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

HAderm by Shanghai Reyoungel Medical Technology Company Limited — Class III — 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

EUDAMED SRN
CN-MF-000010507
Authorised Representative
Luxus Lebenswelt GmbH DE-AR-000005110

Sources (1)

  • EUDAMED 4d48cf68-6b77-4427-81f1-77b72f62ad99 61 fields · synced Jul 9, 2026