Esther
by Ids Ltd.
Ref IDS-UM-0732Model ESTHER
Esther (IDS-UM-0732) is a medical device (EU MDD Class IIb; EMDN category phototherapy equipment) made by Ids Ltd., registered in EUDAMED on 28 Apr 2026 (Basic UDI-DI B-08809578390481), active as of 24 Oct 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-08809578390481 08809578390481 | Date28 Apr 2026 | StatusActive |
Official records
- EUDAMED public site B-08809578390481
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/MDD Active
Specification
- Device name
- Phototherapy Unit
- Model / reference
- ESTHER, IDS-UM-0732
- Primary DI / UDI-DI
- 08809578390481
- Basic UDI-DI
- B-08809578390481
- EMDN code
- Z12040202 Phototherapy equipment
- Device class
- Class IIb
- System or procedure pack
- System which is a device in itself
- EU registration type
- Legacy device (under a directive)
- EU market of registration
- Spain
Manufacturer details
- EUDAMED SRN
- KR-MF-000018259
- Authorised representative
- Obelis s.a. BE-AR-000000106
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