← Back to catalogue
Ampcare ES NMES
EUDAMEDClass IIa (EU MDR)
Ref 50701Model ES NMES
by Ampcare, LLC
Identity
- Trade Name
- Ampcare ES NMES EUDAMED
- Device Name
- Ampcare ES NMES EUDAMED
- Model / Reference
- ES NMES EUDAMED50701 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 00867786000224 EUDAMED
- Basic UDI-DI
- 0867786000250701K5 EUDAMED
- Direct Marketing DI
- 00867786000224 EUDAMED
- EMDN Code
- Z120622 MUSCLE STIMULATORS EUDAMED
Classification
- Device Class
- Class IIa 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
Ampcare ES NMES by Ampcare, LLC — Class IIa — 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 | 0867786000250701K5 | Class IIa | Active |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Ampcare, LLC
- EUDAMED SRN
- US-MF-000038602
- Authorised Representative
- Obelis s.a. BE-AR-000000106
Sources (1)
- EUDAMED 9066682e-fc9d-47e6-b464-78f44ade248f 61 fields · synced Jun 18, 2026