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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
16974162020231 EUDAMED
Basic UDI-DI
B-16974162020231 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 (1)

  • EUDAMED 02dcdd4d-17e1-4e4d-a42b-1b364fd9c038 61 fields · synced Jun 17, 2026