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5.5 x 42CM XL ADVANTAGE LOUPE

by Keeler Ltd 2 variants

Ref 2113-P-2013

Active European Union

CE MDR

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None, self-declared

Class I: no certifier involved

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number50552727LOUPEFRAMEDB Basic UDI-DI 05055272704397UDI-DIDate8 Sep 2023RegisteredStatusActive

Certificates

0 certificates · EUDAMED

No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
Loupes and frames
Model / Reference
2113-P-2013
Primary DI / UDI-DI
05055272704397
Basic UDI-DI
50552727LOUPEFRAMEDB
Direct Marketing DI
05055272704397
EMDN Code
Q0299 Ophthalmic devices - other
Device Class
Class I
EU market of registration
Greece

Manufacturer details

EUDAMED SRN
GB-MF-000009031
Authorised representative
Keeler Europe Distribution, S.L. ES-AR-000001559

Other devices from Keeler Ltd

See all devices from Keeler Ltd →

Properties

Other properties (13)

  • Sterile: No
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: 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