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61166

by Beurer GmbH

Ref 61166Model IL 21 System

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 linked in EUDAMED

A group certificate may exist

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 Number4211125IL21SystemS6 Basic UDI-DI 04211125611668UDI-DIDate8 Oct 2026RegisteredStatusActive

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Model / Reference
IL 21 System, 61166
Primary DI / UDI-DI
04211125611668
Basic UDI-DI
4211125IL21SystemS6
EMDN Code
Z120614 Infrared ultraviolet ray lamps
Device Class
Class IIa
Medical Purpose
The infrared lamp is intended for irradiating the human body. By irradiating with infrared light, heat is transported to the human body.

Manufacturer details

EUDAMED SRN
DE-PR-000033363

Other devices from Beurer GmbH

See all devices from Beurer GmbH →

Properties

Other properties (1)

  • Sterile: No