← Back to catalogue

Monofil

EUDAMED

Class III (EU MDR)

Ref FS27CF

by Assut Europe Spa

Identity

Trade Name
MONOFIL EUDAMED
Device Name
MONOFIL EUDAMED
Model / Reference
FS27CF EUDAMED

Identifiers

Primary DI / UDI-DI
38033439455427 EUDAMED
Basic UDI-DI
8033439MONOFIL3T EUDAMED
Direct Marketing DI
38033439455427 EUDAMED
EMDN Code
H010101010301 POLIGLECAPRONE AND DERIVATIVES MONOFILAMENT WITH NEEDLE 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

Monofil 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

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

Manufacturer

Manufacturer
Assut Europe Spa
EUDAMED SRN
IT-MF-000018178

Sources (1)

  • EUDAMED 6e5062fd-2ae5-4ad6-9af1-4779ebf2556c 61 fields · synced Aug 1, 2026