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Sofiderm

EUDAMED

Class III (EU MDR)

Ref 2.0mlModel Derm Plus

by Hangzhou Techderm Biological Products Co.Ltd

Identity

Trade Name
Sofiderm EUDAMED
Device Name
Cross-linked Sodium Hyaluronate Gel for Plastic Surgery EUDAMED
Model / Reference
Derm Plus EUDAMED
2.0ml EUDAMED

Identifiers

Primary DI / UDI-DI
06924616668093 EUDAMED
Basic UDI-DI
B-06924616668093 EUDAMED
EMDN Code
P900402 RESORBABLE FILLING AND RECONSTRUCTION DEVICES EUDAMED

Classification

Device Class
Class III EUDAMED
Market of Registration
Germany 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

Sofiderm by Hangzhou Techderm Biological Products Co.Ltd — 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-000009378
Authorised Representative
Caretechion GmbH DE-AR-000005946

Sources (1)

  • EUDAMED 9daf4f60-06df-4a80-83f0-a32ce949fef6 61 fields · synced Jun 19, 2026