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Morsetto Doppio Per Fep Grande St

EUDAMED

Class I (EU MDR)

Ref 5000032STModel Morsetto

by Mikai s.p.a.

Identity

Trade Name
MORSETTO DOPPIO PER FEP GRANDE ST EUDAMED
Device Name
FEP EUDAMED
Model / Reference
Morsetto EUDAMED
5000032ST EUDAMED

Identifiers

Primary DI / UDI-DI
08055731435142 EUDAMED
Basic UDI-DI
805573143FEP0000CLAMP.SKT EUDAMED
EMDN Code
P0912040102 AXIAL BONE FIXATION SYSTEMS EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Italy EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMED

Implantable

No

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

Morsetto Doppio Per Fep Grande St by Mikai s.p.a. — 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

Manufacturer
Mikai s.p.a.
EUDAMED SRN
IT-MF-000030732

Sources (1)

  • EUDAMED 8c331036-d96a-43ab-be05-5c163cac7a75 61 fields · synced Jul 9, 2026