Treatment Table

by Medical-Master Co., Ltd. 4 variants

Model ML series

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	Number471987519ML2C Basic UDI-DI 04719875194528UDI-DI	Date26 Jan 2026Registered	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Withdrawn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: ML series

Primary DI / UDI-DI: 04719875194528
Basic UDI-DI: 471987519ML2C
EMDN Code: Z12040299 General medicine therapeutic treatment instruments - other

Device Class: Class I
EU market of registration: Spain

Manufacturer details

EUDAMED SRN: TW-MF-000051361
Authorised representative: RIOMAVIX SOCIEDAD LIMITADA ES-AR-000001202

Other devices from Medical-Master Co., Ltd.

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Class I
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Class I
Patient Stretcher

Class I
Treatment Table

Class I
Treatment Table

Class I
Medical Bed

Class I

See all devices from Medical-Master Co., Ltd. →

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