3 Panel Abdominal Binder

by Chaneco Ltd 5 variants

Ref AB3-XXLModel AB3-L

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 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

Region	Authorization	Number	Date	Status
European Union	CE/MDR	Number50561576AbdominalBnd8R Basic UDI-DI 05056157600049UDI-DI	Date13 Mar 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Withdrawn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: AB3-L, AB3-XXL

Primary DI / UDI-DI: 05056157600049
Basic UDI-DI: 50561576AbdominalBnd8R
EMDN Code: Y060406 Abdominal hernia supports

Device Class: Class I
EU market of registration: Ireland

Manufacturer details

EUDAMED SRN: UK-MF-000043937
Authorised representative: UKALIA Limited XI-AR-000024526

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Properties

Contains Latex

Other properties (12)

Sterile: No
Implantable: No
Reusable: 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