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OneTouch Delica Plus Ace

EUDAMED

Class IIa (EU MDR)

Ref 013-020Model 114301-592

by Asahi Polyslider Company, Limited

Identity

Trade Name
OneTouch Delica Plus Ace EUDAMED
Device Name
OneTouch Delica Plus Lancet EUDAMED
Model / Reference
114301-592 EUDAMED
013-020 EUDAMED

Identifiers

Primary DI / UDI-DI
04580505780738 EUDAMED
Basic UDI-DI
458050578OTDPLANCETMX EUDAMED
Unit of Use DI
84580505780734 EUDAMED
EMDN Code
V010402 LANCETS WITHOUT SAFETY SYSTEMS, SINGLE-USE EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Romania 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 Ace by Asahi Polyslider Company, Limited — Class IIa — MDR — listed in EUDAMED — regulatory data on deviCERTS

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
Emergo Europe B.V. NL-AR-000000116

Sources (1)

  • EUDAMED d291be68-bdcf-49c3-aad6-748ef91805b9 61 fields · synced Jul 17, 2026