← Back to catalogue
Kit Fep Angolare Grande St
EUDAMEDClass IIb (EU MDR)
Ref 5000061MSTModel Kit
by Mikai s.p.a.
Identity
- Trade Name
- KIT FEP ANGOLARE GRANDE ST EUDAMED
- Device Name
- FEP EUDAMED
- Model / Reference
- Kit EUDAMED5000061MST EUDAMED
Identifiers
- Primary DI / UDI-DI
- 08056630554057 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 Angolare 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
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | 805573143FEP000KITFEP.S9R | Class IIb | Active |
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 fb89d3cb-5ebc-4b6c-9dda-d35c9821bc8d 61 fields · synced Jul 17, 2026