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Lanmage

by Shenzhen Lanmage Medical Technology Co., Ltd. 6 variants

Part of a family of 6 devices: see the family page

Ref 9100K1

Lanmage (9100K1) 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 European Union

CE MDR

Valid until

No date given

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Source EUDAMED, synced 7 Nov 2026.

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number697129745001LE Basic UDI-DI 06971297451728UDI-DIDate25 Jul 2025RegisteredStatusActive

Official records

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Device name
Digital X-ray Radiography System
Model / reference
9100K1
Primary DI / UDI-DI
06971297451728
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

Similar devices in this category

Other devices filed under MULTIFUNCTIONAL SYSTEMS FOR DIRECT DIGITAL RADIOLOGY.

Other devices from Shenzhen Lanmage Medical Technology Co., Ltd.

See all devices from Shenzhen Lanmage Medical Technology Co., Ltd. →

Properties

  • Measuring function
Other properties (13, all answered No)