Matrix U24

by IMO - Indústrias Metalúrgicas, S.A.

Ref 945.U24Model MATRIX U24

Active European Union

CE MDR

Valid until

No date given

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 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

Region	Authorization	Number	Date	Status
European Union	CE/MDR	Number5600717213MATRIXU24ES Basic UDI-DI 05600717213202UDI-DI	Date13 Sep 2023Registered	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Withdrawn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: MATRIX U24, 945.U24

Primary DI / UDI-DI: 05600717213202
Basic UDI-DI: 5600717213MATRIXU24ES
Direct marketing DI: 05600717213202
EMDN code: V08060101 Hospital/home care electric medical beds

Device class: Class I
EU registration type: Standard device
EU market of registration: Portugal

Manufacturer details

EUDAMED SRN: PT-MF-000006644

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Properties

Other properties (14)

Supplied sterile: No
Sterilise before use: No
Implantable: No
Reusable: No
Contains latex: No
Reprocessed single-use device: No
Contains CMR substances (carcinogenic, mutagenic or toxic to reproduction): No
Incorporates a substance derived from human blood or plasma: No
Contains human tissues or cells: No
Contains animal tissues or cells: No
Contains endocrine-disrupting substances: No
Administering medicine: No
Measuring function: No
Incorporates a medicinal substance: No