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Kit Fep Minimo St

EUDAMED

Class IIb (EU MDR)

Ref 5000090MSTModel Kit

by Mikai s.p.a.

Identity

Trade Name
KIT FEP MINIMO ST EUDAMED
Device Name
FEP EUDAMED
Model / Reference
Kit EUDAMED
5000090MST EUDAMED

Identifiers

Primary DI / UDI-DI
08056630553982 EUDAMED
Basic UDI-DI
805573143FEP000KITFEP.S9R EUDAMED
EMDN Code
P0912040102 AXIAL BONE FIXATION SYSTEMS EUDAMED

Classification

Device Class
Class IIb EUDAMED
Market of Registration
Italy EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMED

Implantable

Yes

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

Sutures

Yes

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

Kit Fep Minimo St by Mikai s.p.a. — Class IIb — 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 141a58d4-6a5b-4648-82d4-2ca5528c754f 61 fields · synced Jul 14, 2026