← Back to catalogue

OneTouch Delica Plus Lancet

EUDAMED

Class IIa (EU MDR)

Ref 024-017Model 114301-592

by Asahi Polyslider Company, Limited

Identity

Trade Name
OneTouch Delica Plus Lancet EUDAMED
OneTouch Delica Plus Lancetas EUDAMED
Device Name
OTDP Lancet 100 ES/PT EUDAMED
OneTouch Delica Plus Lancet EUDAMED
Model / Reference
114301-592 EUDAMED
024-017 EUDAMED

Identifiers

Primary DI / UDI-DI
04580505780103 EUDAMED
Basic UDI-DI
B-04580505780103 EUDAMED
458050578OTDPLANCETMX EUDAMED
Unit of Use DI
84580505780109 EUDAMED
EMDN Code
V010402 LANCETS WITHOUT SAFETY SYSTEMS, SINGLE-USE EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Spain EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

CMR Substance

Yes

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

OneTouch Delica Plus Lancet by Asahi Polyslider Company, Limited — Class IIa — MDR, MDD — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

European Union Active

CE/MDD

Is this your device? Claim it to add documentation and request validation.

Manufacturer

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

Sources (2)

  • EUDAMED 5af883de-9de8-4783-b148-3652b68fdc3c 61 fields · synced Jun 19, 2026
  • EUDAMED 02462070-5f9d-422a-a879-90c8452222d8 61 fields · synced Jun 19, 2026