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Kit Fep Dinamizzabile Medio St

EUDAMED

Class IIb (EU MDR)

Ref 5000067MSTModel Kit

by Mikai s.p.a.

Identity

Trade Name
KIT FEP DINAMIZZABILE MEDIO ST EUDAMED
Device Name
FEP EUDAMED
Model / Reference
Kit EUDAMED
5000067MST EUDAMED

Identifiers

Primary DI / UDI-DI
08056630554088 EUDAMED
Basic UDI-DI
805573143FEP000KITFEP.S9R EUDAMED
EMDN Code
P09120499 EXTERNAL BONE FIXATION SYSTEMS - OTHER 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 Dinamizzabile Medio 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 37292b41-47ef-47be-a613-015ec3f846e3 61 fields · synced Sep 17, 2026