M30
by Mediana Co., Ltd 4 variants
Ref M30M-1NHModel M30
M30 (M30M-1NH) is a Class IIb device made by Mediana Co., Ltd., registered in EUDAMED on 15 May 2026 (Basic UDI-DI B-18800003418265), 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-18800003418265 18800003418265 | Date15 May 2026 | StatusActive |
Official records
- EUDAMED public site B-18800003418265
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/MDD Active
Specification
- Device name
- Multi-Parameter Patient Monitor
- Model / reference
- M30, M30M-1NH
- Primary DI / UDI-DI
- 18800003418265
- Basic UDI-DI
- B-18800003418265
- EMDN code
- Z1203020201 Multi–parameter patient bedside monitors
- Device class
- Class IIb
- EU registration type
- Legacy device (under a directive)
- EU market of registration
- Spain
Manufacturer details
- EUDAMED SRN
- KR-MF-000026570
- Authorised representative
- Obelis s.a. BE-AR-000000106
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