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Medoject Fine

EUDAMED

Class IIa (EU MDR)

Ref 805.M3106.DS.VTModel MOWANA

by Pentamaster MediQ Sdn. Bhd.

Identity

Trade Name
MEDOJECT FINE EUDAMED
Device Name
Hypodermic Pen Needles EUDAMED
Model / Reference
MOWANA EUDAMED
805.M3106.DS.VT EUDAMED

Identifiers

Primary DI / UDI-DI
09551014892088 EUDAMED
Basic UDI-DI
955101489PENNEEDLEPS EUDAMED
Direct Marketing DI
09551014892088 EUDAMED
EMDN Code
A0101010201 HYPODERMIC PEN NEEDLES, WITH SAFETY SYSTEMS EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Slovakia 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

Medoject Fine by Pentamaster MediQ Sdn. Bhd. — 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
MY-MF-000049132
Authorised Representative
Europecert UG (haftungsbeschränkt) DE-AR-000004974

Sources (1)

  • EUDAMED 71356394-3c58-4a0f-83b8-391b8291e1d0 61 fields · synced Jun 18, 2026