← Back to catalogue

GBUK Silicone Foam

EUDAMED

Class IIb (EU MDR)

Ref SF2020Model foam

by Zhejiang Hongyu Medical Commodity Co., Ltd

Identity

Trade Name
GBUK Silicone Foam EUDAMED
Device Name
silicone dressings EUDAMED
Model / Reference
foam EUDAMED
SF2020 EUDAMED

Identifiers

Primary DI / UDI-DI
06938056216127 EUDAMED
Basic UDI-DI
69380562SD002NA EUDAMED
EMDN Code
M04040701 SILICONE DRESSINGS, NON-COMBINED EUDAMED

Classification

Device Class
Class IIb EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

GBUK Silicone Foam by Zhejiang Hongyu Medical Commodity Co., Ltd — Class IIb — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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

Manufacturer

EUDAMED SRN
CN-MF-000008204
Authorised Representative
RIOMAVIX SOCIEDAD LIMITADA ES-AR-000001202

Sources (1)

  • EUDAMED 1552612e-0d27-4d76-a259-d6719ca59e5d 61 fields · synced Jun 17, 2026