← Back to catalogue

Kit Fep Dinamizzabile Grande St

EUDAMED

Class IIb (EU MDR)

Ref 5000068MSTModel Kit

by Mikai s.p.a.

Identity

Trade Name
KIT FEP DINAMIZZABILE GRANDE ST EUDAMED
Device Name
FEP EUDAMED
Model / Reference
Kit EUDAMED
5000068MST EUDAMED

Identifiers

Primary DI / UDI-DI
08056630554095 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 Grande 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

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

Manufacturer

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

Sources (1)

  • EUDAMED 9a444e11-4794-49e1-824a-0932d90be2bd 61 fields · synced Sep 18, 2026