Ampcare ES NMES
by Ampcare, LLC
Ref 50701Model ES NMES
Ampcare ES NMES (50701) is a medical device (EU MDR Class IIa; EMDN category muscle stimulators) made by Ampcare, LLC, registered in EUDAMED on 21 Apr 2026 (Basic UDI-DI 0867786000250701K5) with CE/MDR certificate 28620211194-01 valid until 24 Feb 2030, active as of 22 Oct 2026.
Active
CE MDR
Valid until
24 Feb 2030
FDA recalls
Not applicable
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR | Number28620211194-01 | Date4 Aug 2026 | StatusActive |
Official records
- EUDAMED public site 0867786000250701K5
Certificates
- 28620211194-01 Active
Quality management system EU MDR
- Certifier
- Intertek Medical Notified Body AB 2862
- Issued
- 4 Aug 2026
- Expires
- 24 Feb 2030
- Reason
- Other
Timeline
- Registered EUDAMED 0867786000250701K5
- Certificate issued EUDAMED 28620211194-01
- Certificate expires EUDAMED 28620211194-01
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/MDR Active
Specification
- Model / reference
- ES NMES, 50701
- Primary DI / UDI-DI
- 00867786000224
- Basic UDI-DI
- 0867786000250701K5
- Direct marketing DI
- 00867786000224
- EMDN code
- Z120622 Muscle stimulators
- Device class
- Class IIa
- EU registration type
- Standard device
- EU market of registration
- Ireland
Manufacturer details
- EUDAMED SRN
- US-MF-000038602
- Authorised representative
- Obelis s.a. BE-AR-000000106
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