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Alternating-pressu ire bed mattress system

EUDAMED

Class IIa (EU MDR)

Ref ARMONYII500Model Virgo-+Effect 5200

by Airflo (Xiamen) Medical Co., Ltd

Identity

Device Name
Alternating-pressu ire bed mattress system EUDAMED
Model / Reference
Virgo-+Effect 5200 EUDAMED
ARMONYII500 EUDAMED

Identifiers

Primary DI / UDI-DI
06972910601964 EUDAMED
Basic UDI-DI
B-06972910601964 EUDAMED
EMDN Code
V080702 NON ACTIVE ANTI-DECUBITUS MEDICAL MATTRESSES EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
France EUDAMED

Clinical & Handling

Sterile

No

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

Alternating-pressu ire bed mattress system by Airflo (Xiamen) Medical Co., 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
CN-MF-000008552
Authorised Representative
Share info GmbH DE-AR-000005132

Sources (1)

  • EUDAMED 54138220-81ef-4e59-8f81-e1a9c2df33a6 61 fields · synced Jun 20, 2026