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Assumesh

EUDAMED

Class III (EU MDR)

Ref AM0510APFV03

by Assut Europe Spa

Identity

Trade Name
ASSUMESH EUDAMED
Device Name
ASSUMESH EUDAMED
Model / Reference
AM0510APFV03 EUDAMED

Identifiers

Primary DI / UDI-DI
58033439435812 EUDAMED
Basic UDI-DI
8033439ASSUMESHBP EUDAMED
Direct Marketing DI
58033439435812 EUDAMED
EMDN Code
P900202 POLYPROPYLENE SURGICAL MESHES EUDAMED

Classification

Device Class
Class III EUDAMED
Market of Registration
Italy EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMED

Implantable

Yes

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

Assumesh by Assut Europe Spa — Class III — 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

Manufacturer
Assut Europe Spa
EUDAMED SRN
IT-MF-000018178

Sources (1)

  • EUDAMED 87a22e61-0677-4dc1-8c87-c2829d978fd5 61 fields · synced Aug 1, 2026