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Hydroven

EUDAMED

Class IIa (EU MDR)

Ref 510004DEModel 526000-03

by ArjoHuntleigh AB

Identity

Trade Name
HYDROVEN EUDAMED
Device Name
ACS900 PUMP UK STD TUBE SET EUDAMED
Model / Reference
526000-03 EUDAMED
510004DE EUDAMED

Identifiers

Primary DI / UDI-DI
05051968031938 EUDAMED
Basic UDI-DI
5060693520013VG EUDAMED
EMDN Code
Z120607 PNEUMATIC COMPRESSION EQUIPMENT EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Ireland 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

Hydroven by Arjohuntleigh AB — 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

Manufacturer
ArjoHuntleigh AB
EUDAMED SRN
SE-MF-000000696

Sources (1)

  • EUDAMED fb74cd26-acc5-4ba0-a76c-6c314c9bd5c9 61 fields · synced Jun 19, 2026