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Vhenus 2

EUDAMED

Class I (EU MDR)

Ref VHCB000/000Model 120PM000/000Ref VH000/000

by ArjoHuntleigh AB

Identity

Trade Name
Vhenus 2 EUDAMED
Device Name
Pentaflex EUDAMED
Model / Reference
120PM000/000 EUDAMED
VHCB000/000 EUDAMED
VH000/000 EUDAMED

Identifiers

Primary DI / UDI-DI
05056341676119 EUDAMED
05056341676102 EUDAMED
Basic UDI-DI
5060693520174W9 EUDAMED
EMDN Code
V080702 NON ACTIVE ANTI-DECUBITUS MEDICAL MATTRESSES EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
France 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

Vhenus 2 by Arjohuntleigh AB — 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
ArjoHuntleigh AB
EUDAMED SRN
SE-MF-000000696

Sources (2)

  • EUDAMED 66ed4c32-d213-446c-ada2-dd27df972307 61 fields · synced Jun 20, 2026
  • EUDAMED c305c9d2-9952-40af-abe1-32b90436a1fe 61 fields · synced May 19, 2026