Identity
- Trade Name
- Salmonella Paratyphi AH EUDAMED
- Device Name
- Salmonella Paratyphi AH EUDAMED
- Model / Reference
- 5050 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 08053172971618 EUDAMED
- Basic UDI-DI
- B-08053172971618 EUDAMED
- EMDN Code
- W0105011002 SALMONELLA ANTIBODY ASSAYS EUDAMED
Classification
- Device Class
- Class IVD General EUDAMED
- Market of Registration
- Italy EUDAMED
Clinical & Handling
Sterile
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
Yes
EUDAMED
Microbial Substances
Yes
EUDAMED
Reagent
Yes
EUDAMED
Self Testing
No
EUDAMED
Near-Patient Testing
No
EUDAMED
Professional Testing
Yes
EUDAMED
Companion Diagnostics
No
EUDAMED
Surgical Instrument
No
EUDAMED
Salmonella Paratyphi AH by Giesse Diagnostics Srl — Class IVD General — IVDD — listed in EUDAMED — regulatory data on deviCERTS
Authorization Coverage (European Union — 27 member states)
Regulatory Authorizations
European Union Active
CE/IVDD
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/IVDD | B-08053172971618 | Class IVD General | Active |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Giesse Diagnostics Srl
- EUDAMED SRN
- IT-MF-000039031
Sources (1)
- EUDAMED baa617cf-6c38-4a17-9143-6d97c73710b8 61 fields · synced Jun 18, 2026