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Circus LED

by Glamox AS 19 variants

Ref Circus LED M T100 AWh 600 940 3,5D CLA BT EU

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 Number704067CIRCUSLEDJM Basic UDI-DI 07040670282972UDI-DIDate5 Aug 2026RegisteredStatusActive

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  • Withdrawn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
Circus LED
Model / Reference
Circus LED M T100 AWh 600 940 3, 5D CLA BT EU
Primary DI / UDI-DI
07040670282972
Basic UDI-DI
704067CIRCUSLEDJM
Direct Marketing DI
07040670282972
EMDN Code
Z120499 General medicine instruments - other
Device Class
Class I
EU market of registration
Norway

Manufacturer details

EUDAMED SRN
NO-MF-000052034

Other devices from Glamox AS

See all devices from Glamox AS →

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