Canule de Charleux 23G

by Laboratoire De Contactologie Appliquee - Lca

Ref R5020CModel RHEXIS Canule

Active European Union

CE MDD

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None linked in EUDAMED

A group certificate may exist

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/MDD	NumberB-03700288635365 Basic UDI-DI 03700288635365UDI-DI	Date6 Mar 2026Registered	StatusActive

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

European Union — CE/MDD Active

Specification

EUDAMED

Device Name: Canule de Charleux 23G - Boite de 100
Model / Reference: RHEXIS Canule, R5020C

Primary DI / UDI-DI: 03700288635365
Basic UDI-DI: B-03700288635365
EMDN Code: Q021101 Occular irrigation and aspiration cannulas, single-use

Device Class: Class IIa
EU market of registration: France

Manufacturer details

EUDAMED SRN: FR-MF-000001732

Other devices from Laboratoire De Contactologie Appliquee - Lca

Ixium Naha 1, 5%

Class IIb
Arthrum H 2%

Class III
Coque oculaire transparente

Class I
Synovium Hcs

Class III
PHYLARM 2mL

Class I
Hyaline

Class IIb

See all devices from Laboratoire De Contactologie Appliquee - Lca →

Properties

Sterile

Other properties (10)

Implantable: No
Reusable: No
Contains Latex: No
Reprocessed: No
Human-derived: No
Human Tissues: No
Animal Tissues: No
Administering Medicine: No
Measuring Function: No
Incorporates Medicinal Product: No