← Back to catalogue
Kit Procedure Diagnostiche/Interventistiche
EUDAMEDClass IIa (EU MDR)
Ref 891396/RModel CUSTOM KIT
Identity
- Device Name
- KIT PROCEDURE DIAGNOSTICHE/INTERVENTISTICHE EUDAMED
- Model / Reference
- CUSTOM KIT EUDAMED891396/R EUDAMED
Identifiers
- Primary DI / UDI-DI
- D-891396/RH9 EUDAMED
- Basic UDI-DI
- B-891396/RH9 EUDAMED
- EMDN Code
- T0202 SURGICAL PROCEDURAL KITS (EXCLUDING SURGICAL INSTRUMENT KITS) 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
Yes
EUDAMED
Measuring Function
No
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
Kit Procedure Diagnostiche/Interventistiche by Med Italia Biomedica 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-891396/RH9 | Class IIa | Active |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Med Italia Biomedica S.r.l
- EUDAMED SRN
- IT-MF-000025272
Sources (1)
- EUDAMED 55fb0ddc-1955-480c-af1f-df1fc836933f 61 fields · synced Oct 6, 2026