Identity
- Trade Name
- Test-It EUDAMED
- Device Name
- Switch Interfaces EUDAMED
- Model / Reference
- Test-It EUDAMED
Identifiers
- Primary DI / UDI-DI
- 05060895630602 EUDAMED
- Basic UDI-DI
- 506089563INT1DN EUDAMED
- Direct Marketing DI
- 05060895630602 EUDAMED
- EMDN Code
- Y210999,Y214299,Y240999,Y241899 EUDAMED
Classification
- Device Class
- Class I EUDAMED
- Market of Registration
- Ireland EUDAMED
Clinical & Handling
Sterile
No
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
Test-It by Pretorian Technologies Ltd — Class I — 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 | 506089563INT1DN | Class I | Active |
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Manufacturer
- Manufacturer
- Pretorian Technologies Ltd
- EUDAMED SRN
- GB-MF-000008344
- Authorised Representative
- European Healthcare & Device Solutions Ltd. IE-AR-000003999
Sources (1)
- EUDAMED 312c62e7-dcfd-4822-aafe-6ba198094c5e 61 fields · synced Oct 6, 2026