Lanmage
by Shenzhen Lanmage Medical Technology Co., Ltd. 6 variants
Part of a family of 6 devices: see the family page
Ref 9100K
Lanmage (9100K) is a Class IIb device made by Shenzhen Lanmage Medical Technology Co., Ltd., registered in EUDAMED on 25 Jul 2025 (Basic UDI-DI 697129745001LE), active as of 7 Nov 2026.
Active
CE MDR
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/MDR | Number697129745001LE 06971297451582 | Date25 Jul 2025 | StatusActive |
Official records
- EUDAMED public site 697129745001LE
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/MDR Active
Specification
- Device name
- Digital X-ray Radiography System
- Model / reference
- 9100K
- Primary DI / UDI-DI
- 06971297451582
- Basic UDI-DI
- 697129745001LE
- EMDN code
- Z11031101 Multifunctional systems for direct digital radiology
- Device class
- Class IIb
- System or procedure pack
- System which is a device in itself
- EU registration type
- Standard device
- EU market of registration
- Ireland
Manufacturer details
- EUDAMED SRN
- CN-MF-000001122
- Authorised representative
- Lotus NL B.V. NL-AR-000000121
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