Cinto erniario doppio

by G.L.O. SRL 10 variants

Ref 582

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 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

Region	Authorization	Number	Date	Status
European Union	CE/MDR	Number805156628582DJ Basic UDI-DI 08051566288403UDI-DI	Date21 Nov 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Withdrawn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

Device Name: Cinto erniario doppio
Model / Reference: 582

Primary DI / UDI-DI: 08051566288403
Basic UDI-DI: 805156628582DJ
EMDN Code: Y060406 Abdominal hernia supports

Device Class: Class I
EU market of registration: Italy

Manufacturer details

EUDAMED SRN: IT-MF-000018554

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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