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Kd-Fine Safety

EUDAMED

Class IIa (EU MDR)

Ref 911693B

by KD Medical GmbH Hospital Products

Identity

Trade Name
KD-FINE SAFETY EUDAMED
Device Name
KD-FINE Hypodermic Needles EUDAMED
Model / Reference
911693B EUDAMED

Identifiers

Primary DI / UDI-DI
74031881911692 EUDAMED
Basic UDI-DI
4031881G10-01IIaKB EUDAMED
EMDN Code
A0101010101 HYPODERMIC SYRINGE NEEDLES, WITH SAFETY SYSTEMS EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Poland 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

Category: Hypodermic needle, single-use

Kd-Fine Safety by KD Medical GmbH Hospital Products — Class IIa — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Hypodermic needle, single-use.

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 09c048ce-ab0d-44a0-83c4-5a01d39f219e 61 fields · synced Jun 17, 2026