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Kd-Ject E

EUDAMED

Class I (EU MDR)

Ref 875674

by KD Medical GmbH Hospital Products

Identity

Trade Name
KD-JECT E EUDAMED
Device Name
KD-JECT E EUDAMED
Model / Reference
875674 EUDAMED

Identifiers

Primary DI / UDI-DI
24031881875678 EUDAMED
Basic UDI-DI
4031881G11-02bImsZQ EUDAMED
EMDN Code
A020108 ENTERAL FEEDING SYRINGES EUDAMED

Classification

Device Class
Class I 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

Yes

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Kd-Ject E by KD Medical GmbH Hospital Products — Class I — 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 f7554427-e380-4add-bd3e-501cd7e0b7a8 61 fields · synced Jun 19, 2026