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ArmFlow

EUDAMED

Class I (EU MDR)

Ref NA

by Articares Pte Ltd

Identity

Trade Name
ArmFlow EUDAMED
Device Name
ArmFlow EUDAMED
Model / Reference
NA EUDAMED

Identifiers

Primary DI / UDI-DI
08885020070033 EUDAMED
Basic UDI-DI
888502007AFV10MBM EUDAMED
EMDN Code
Z12069080 VARIOUS PHYSIOTHERAPY AND REHABILITATION INSTRUMENTS - HARDWARE ACCESSORIES EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

No

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

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

ArmFlow by Articares Pte Ltd — 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

Manufacturer
Articares Pte Ltd
EUDAMED SRN
SG-MF-000008179
Authorised Representative
QAdvis EAR AB SE-AR-000001599

Sources (1)

  • EUDAMED b4f84c30-6939-4546-b02f-e84efd8214ac 61 fields · synced Jun 18, 2026