Ortopedyczny materac hybrydowy Osaka Grid

by Onsen Sp. z o.o. 8 variants

Ref 5907497231427Model 160x200 + Purotex

Active European Union

CE MDR

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None, self-declared

Class I: no certifier involved

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

Region	Authorization	Number	Date	Status
European Union	CE/MDR	Number5907497231OG160PA8 Basic UDI-DI 59074972314270UDI-DI	Date12 Dec 2025Registered	StatusActive

Certificates

0 certificates · EUDAMED

No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Model / Reference: 160x200 + Purotex, 5907497231427

Primary DI / UDI-DI: 59074972314270
Basic UDI-DI: 5907497231OG160PA8
EMDN Code: V080702 Non active anti-decubitus medical mattresses

Device Class: Class I
EU market of registration: Poland

Manufacturer details

EUDAMED SRN: PL-MF-000037523

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Properties

Other properties (13)

Sterile: No
Implantable: No
Reusable: No
Contains Latex: No
Reprocessed: No
CMR Substance: No
Human-derived: No
Human Tissues: No
Animal Tissues: No
Endocrine Disruptor: No
Administering Medicine: No
Measuring Function: No
Incorporates Medicinal Product: No