Identity
- Device Name
- Ago per iniezioni 16G 55mm EUDAMED
- Model / Reference
- CROSSFLEX EUDAMED
Identifiers
- Primary DI / UDI-DI
- 08055348434163 EUDAMED
- Basic UDI-DI
- B-08055348434163 EUDAMED
- EMDN Code
- K0104 VERESS NEEDLES 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
Human-derived
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Administering Medicine
No
EUDAMED
Measuring Function
No
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
Ago per iniezioni 16G 55mm by Meika Group S.r.l. — Class IIa — MDD — listed in EUDAMED — regulatory data on deviCERTS
Authorization Coverage (European Union — 27 member states)
Regulatory Authorizations
European Union Active
CE/MDD
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDD | B-08055348434163 | Class IIa | Active |
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Manufacturer
- Manufacturer
- Meika Group S.r.l.
- EUDAMED SRN
- IT-MF-000029106
Sources (1)
- EUDAMED 834a7833-37b5-4bd6-99c6-04dccb3f9f30 61 fields · synced Jun 19, 2026