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ReCure Elektrodenpad
EUDAMEDClass IIb (EU MDR)
Ref PAD-003Model EXA-001
by Aneuvo
Identity
- Trade Name
- ReCure Elektrodenpad EUDAMED
- Device Name
- ExaStim Stimulation System EUDAMED
- Model / Reference
- EXA-001 EUDAMEDPAD-003 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 00850053287145 EUDAMED
- Basic UDI-DI
- 0850053287EXSYYU EUDAMED
- EMDN Code
- Z120601 ELECTROTHERAPY EQUIPMENT (INCLUDED TENS) EUDAMED
Classification
- Device Class
- Class IIb EUDAMED
- Market of Registration
- Germany 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
ReCure Elektrodenpad by Aneuvo — Class IIb — 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 | 0850053287EXSYYU | Class IIb | Active |
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Manufacturer
- Manufacturer
- Aneuvo
- EUDAMED SRN
- US-MF-000041520
- Authorised Representative
- Obelis s.a. BE-AR-000000106
Sources (1)
- EUDAMED f38cdead-880a-4d42-b188-f73b457d01d6 61 fields · synced Aug 4, 2026