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OneTouch Delica Plus Lancing Device

by Asahi Polyslider Company, Limited 5 variants

Ref 023-982Model 114303-593

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 Number458050578OTDPDEVICEMM Basic UDI-DI 04580505780332UDI-DIDate31 May 2022RegisteredStatusActive

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  • Withdrawn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

Model / Reference
114303-593, 023-982
Primary DI / UDI-DI
04580505780332
Basic UDI-DI
458050578OTDPDEVICEMM
EMDN Code
V9099 Various devices not included in other classes - other
Device Class
Class I
EU market of registration
Czechia

Manufacturer details

EUDAMED SRN
JP-MF-000009245
Authorised representative
LifeScan Deutschland GmbH DE-AR-000005105

Related devices

Category: Device sterilization/disinfection container, reusable

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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