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Kd-Penofine

EUDAMED

Class IIa (EU MDR)

Ref 907023T

by KD Medical GmbH Hospital Products

Identity

Trade Name
KD-PENOFINE EUDAMED
Device Name
KD-PENOFINE Pen Needles EUDAMED
Model / Reference
907023T EUDAMED

Identifiers

Primary DI / UDI-DI
54031881907028 EUDAMED
Basic UDI-DI
4031881G10-02aIIaUV EUDAMED
EMDN Code
A0101010202 HYPODERMIC PEN NEEDLES, W/O SAFETY SYSTEMS EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Sweden EUDAMED

Clinical & Handling

Sterile

Yes

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

Yes

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Kd-Penofine by KD Medical GmbH Hospital Products — 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
DE-MF-000006773

Sources (1)

  • EUDAMED cb882df6-96a2-462c-934b-0c879d22bbdf 61 fields · synced Oct 7, 2026