StimyEcho
Ref AEQN22080
StimyEcho (AEQN22080) is a Class IIa device made by M.D.L. S.R.L., registered in EUDAMED on 22 Oct 2026 (Basic UDI-DI B-08055271577449), active as of 7 Nov 2026.
Active
CE MDD
Valid until
No date given
FDA recalls
Not applicable
Documents
None linked in EUDAMED
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDD | NumberB-08055271577449 08055271577449 | Date22 Oct 2026 | StatusActive |
Official records
- EUDAMED public site B-08055271577449
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/MDD Active
Specification
- Model / reference
- AEQN22080
- Primary DI / UDI-DI
- 08055271577449
- Basic UDI-DI
- B-08055271577449
- EMDN code
- A010302 Plexus block needles and kits
- Device class
- Class IIa
- EU registration type
- Legacy device (under a directive)
- EU market of registration
- Austria
Manufacturer details
- EUDAMED SRN
- IT-MF-000011599
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