Identity
- Trade Name
- master diagnóstica EUDAMED
- Device Name
- pH 9.0 Pre-Treatment Kit EUDAMED
- Model / Reference
- MAD-004075R/200 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 08435421210714 EUDAMED
- Basic UDI-DI
- 8435421200489YN EUDAMED
- Direct Marketing DI
- 08435421210714 EUDAMED
- EMDN Code
- W01030799 HISTOLOGY / CYTOLOGY REAGENTS - OTHER EUDAMED
Classification
- Device Class
- Class A EUDAMED
- Market of Registration
- Spain EUDAMED
Clinical & Handling
Sterile
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Microbial Substances
No
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
New Device
No
EUDAMED
master diagnóstica by Vitro, S.a. — Class A — IVDR — listed in EUDAMED — regulatory data on deviCERTS
Authorization Coverage (European Union — 27 member states)
Regulatory Authorizations
European Union Active
CE/IVDR
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/IVDR | 8435421200489YN | Class A | Active |
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Manufacturer
- Manufacturer
- Vitro, S.a.
- EUDAMED SRN
- ES-MF-000001498
Sources (1)
- EUDAMED 75546d00-bb17-42b8-aee6-618c7efd36a7 61 fields · synced Jun 19, 2026