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Kd-Fine

EUDAMED

Class IIa (EU MDR)

Ref 900390

by KD Medical GmbH Hospital Products

Identity

Trade Name
KD-FINE EUDAMED
Device Name
KD-FINE Hypodermic Needles EUDAMED
Model / Reference
900390 EUDAMED

Identifiers

Primary DI / UDI-DI
24031881900394 EUDAMED
Basic UDI-DI
4031881G10-01IIaKB EUDAMED
EMDN Code
A0101010102 HYPODERMIC SYRINGE NEEDLES, W/O 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

Kd-Fine 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 8bde3074-7752-4098-903e-c884e5ab3400 61 fields · synced Oct 6, 2026