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Perforatore Amniotico

EUDAMED

Class IIa (EU MDR)

Ref Curved

by Yangzhou Wuyang Medical Equipment Co., Ltd.

Identity

Trade Name
PERFORATORE AMNIOTICO EUDAMED
Device Name
Amniotic Membrane Perforators EUDAMED
Model / Reference
Curved EUDAMED

Identifiers

Primary DI / UDI-DI
06974162020302 EUDAMED
26974162020269 EUDAMED
Basic UDI-DI
B-06974162020302 EUDAMED
B-26974162020269 EUDAMED
EMDN Code
U1005 AMNIOTIC MEMBRANE PERFORATORS EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Italy EUDAMED

Clinical & Handling

Sterile

Yes

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

Perforatore Amniotico by Yangzhou Wuyang Medical Equipment Co., Ltd. — Class IIa — 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-000036875
Authorised Representative
SUNGO Europe B.V. NL-AR-000000247

Sources (2)

  • EUDAMED b222888e-2976-42e4-8f38-195280c9df76 61 fields · synced Oct 6, 2026
  • EUDAMED e9c80766-809d-42e0-932d-62a49d3c538d 61 fields · synced May 19, 2026