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Kit Fep Ibrido Medio St
EUDAMEDClass IIb (EU MDR)
Ref 5000001IMSTModel Kit
by Mikai s.p.a.
Identity
- Trade Name
- KIT FEP IBRIDO MEDIO ST EUDAMED
- Device Name
- FEP EUDAMED
- Model / Reference
- Kit EUDAMED5000001IMST EUDAMED
Identifiers
- Primary DI / UDI-DI
- 08056630553999 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 Ibrido 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
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | 805573143FEP000KITFEP.S9R | Class IIb | Active |
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Manufacturer
- Manufacturer
- Mikai s.p.a.
- EUDAMED SRN
- IT-MF-000030732
Sources (1)
- EUDAMED 7e445348-0e0e-4b61-9e98-caf6c8b3dcb3 61 fields · synced Jul 11, 2026