← Back to catalogue
Puntali Per Testiera Mayfield
EUDAMEDClass IIa (EU MDR)
Ref CRO4003Model CROSSFLEX
Identity
- Device Name
- PUNTALI PER TESTIERA MAYFIELD EUDAMED
- Model / Reference
- CROSSFLEX EUDAMEDCRO4003 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 08055348433197 EUDAMED
- Basic UDI-DI
- 805534843FT02CROMAYNG EUDAMED
- EMDN Code
- Z12109099 VARIOUS NEUROLOGY AND NEUROSURGERY INSTRUMENTS - OTHER EUDAMED
Classification
- Device Class
- Class IIa EUDAMED
- Market of Registration
- Italy EUDAMED
Clinical & Handling
Sterile
Yes
EUDAMED
Implantable
No
EUDAMED
Reusable
No
EUDAMED
Contains Latex
No
EUDAMED
Reprocessed
No
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
Puntali Per Testiera Mayfield by Meika Group S.r.l. — Class IIa — 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 | 805534843FT02CROMAYNG | Class IIa | Active |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Meika Group S.r.l.
- EUDAMED SRN
- IT-MF-000029106
Sources (1)
- EUDAMED fb49fceb-8897-4615-9f1c-298b81b76c42 61 fields · synced Jun 19, 2026