Bandage herniaire GIBORTHO T2

Ref 6089-2

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	Number332254063KW Basic UDI-DI 03322546301975UDI-DI	Date13 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Withdrawn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

Device Name: Bandage herniaire GIBORTHO T1
Model / Reference: 6089-2

Primary DI / UDI-DI: 03322546301975
Basic UDI-DI: 332254063KW
Direct Marketing DI: 03322546301975
EMDN Code: Y060406 Abdominal hernia supports

Device Class: Class I
EU market of registration: France

Manufacturer details

EUDAMED SRN: FR-MF-000014279

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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