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Max Vision®Toric

by Eyebright Medical Technology (Beijing) Co., Ltd. 1,000+ variants

Ref AM2T2UXL24,+9.5DModel AMTUXL

Active European Union

CE MDR CE MDD

Valid until

25 Aug 2031

CE MDR certificate

FDA recalls

Not applicable

No FDA record for this device

Documents

1 certificate

Certifier TÜV SÜD Product Service GmbH

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 7 Nov 2026. What this means

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR NumberB-06941264916208 Basic UDI-DI 06941264916208UDI-DIDate27 Mar 2026RegisteredStatusActive
European UnionCE/MDD NumberB-06941264916208 Basic UDI-DI 06941264916208UDI-DIDate27 Mar 2026RegisteredStatusActive

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR, CE/MDD Active

Specification

EUDAMED

Device Name
Preloaded Intraocular Lens System
Model / Reference
AM2T2UXL24, +9.5D, AMTUXL
Primary DI / UDI-DI
06941264916208
Basic UDI-DI
B-06941264916208, 69528868B015SA
EMDN Code
P030102100301 IOLs, APHAKIC, MULTIFOCAL, TORIC, HYDROPHOBIC ACRYLIC
Device Class
Class IIb
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
CN-MF-000003041
Authorised representative
Lotus NL B.V. NL-AR-000000121

Other devices from Eyebright Medical Technology (Beijing) Co., Ltd.

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Properties

  • Sterile
  • Implantable

Other properties (12)

  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • Sutures: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No