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Nasenpflaster

EUDAMED

Class I (EU MDR)

Ref HY2027-9

by Zhejiang Hongyu Medical Commodity Co., Ltd

Identity

Trade Name
Nasenpflaster EUDAMED
Device Name
Nasal Plaster EUDAMED
Model / Reference
HY2027-9 EUDAMED

Identifiers

Primary DI / UDI-DI
06938056233728 EUDAMED
Basic UDI-DI
69380562NP0001J7 EUDAMED
Unit of Use DI
86938056233724 EUDAMED
EMDN Code
M040701 NASAL PADS EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

Yes

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

Nasenpflaster by Zhejiang Hongyu Medical Commodity Co., Ltd — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

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

Sources (1)

  • EUDAMED 1bdfcd8f-f0f7-4169-bf7b-b168e1e22ff4 61 fields · synced Sep 18, 2026