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HEMO PHENIX A.V. Fistula Needle Set

EUDAMED

Class IIa (EU MDR)

Ref A16R25B30SP+Model 862-1641

by JMS Singapore Pte Ltd

Identity

Trade Name
HEMO PHENIX A.V. Fistula Needle Set EUDAMED
Device Name
HEMO PHENIX AVF EUDAMED
Model / Reference
862-1641 EUDAMED
A16R25B30SP+ EUDAMED

Identifiers

Primary DI / UDI-DI
D-862-1641AQ EUDAMED
Basic UDI-DI
B-862-1641AQ EUDAMED
EMDN Code
A010401 ARTERIOVENOUS FISTULA NEEDLES EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
France EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

HEMO PHENIX A.V. Fistula Needle Set by Jms Singapore Pte Ltd — Class IIa — MDD — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

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Manufacturer

EUDAMED SRN
SG-MF-000024704
Authorised Representative
Bionic Medizintechnik GmbH DE-AR-000012049

Sources (1)

  • EUDAMED 29c84034-47a7-4834-8af6-5569d68af86e 61 fields · synced Jun 19, 2026