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Air Mattress cococia Fūka

EUDAMED

Class I (EU MDR)

Ref KE-959E3

by Paramount Bed Co., Ltd.

Identity

Trade Name
Air Mattress cococia Fūka EUDAMED
Device Name
Air Mattress cococia Fūka EUDAMED
Model / Reference
KE-959E3 EUDAMED

Identifiers

Primary DI / UDI-DI
04527799702114 EUDAMED
Basic UDI-DI
4527799TD69D00204BQ EUDAMED
EMDN Code
V080701 ACTIVE ANTI-DECUBITUS MEDICAL MATTRESSES EUDAMED

Classification

Device Class
Class I 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

Air Mattress cococia Fūka by Paramount Bed Co., 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

EUDAMED SRN
JP-MF-000002285
Authorised Representative
Emergo Europe B.V. NL-AR-000000116

Sources (1)

  • EUDAMED 14385d5a-5bb4-49bb-9975-b791fc4074fd 61 fields · synced Jun 18, 2026