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OneTouch Delica Plus Lancing Device

EUDAMED

Class I (EU MDR)

Ref 023-978Model 114303-593

by Asahi Polyslider Company, Limited

Identity

Trade Name
OneTouch Delica Plus Lancing Device EUDAMED
Device Name
OneTouch Delica Plus Lancing Device EUDAMED
Model / Reference
114303-593 EUDAMED
023-978 EUDAMED

Identifiers

Primary DI / UDI-DI
04580505780295 EUDAMED
Basic UDI-DI
458050578OTDPDEVICEMM EUDAMED
EMDN Code
V9099 VARIOUS DEVICES NOT INCLUDED IN OTHER CLASSES - OTHER EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Italy EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Category: Device sterilization/disinfection container, reusable

OneTouch Delica Plus Lancing Device by Asahi Polyslider Company, Limited — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Device sterilization/disinfection container, reusable.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

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

Sources (1)

  • EUDAMED a658377c-b0ee-416a-b632-7b4ab7e01399 61 fields · synced May 22, 2026