Monoart® Cannula EM19 EM19 Aspirator Tip EM19 Absaugkanüle

by Euronda S.P.A.

Ref 22910XXXModel MONOART® CANNULA EM19 EM19 ASPIRATOR TIP EM19 ABSAUGKANÜLE

Withdrawn Withdrawn in European Union. No longer placed on the EU market.

Was authorized under CE MDD

Ended

Withdrawn

Date not published (CE MDD)

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-EM19ASPIRATORTIPTC Basic UDI-DI D-EM19ASPIRATORTIPTCUDI-DI	Date29 Oct 2021Registered	StatusWithdrawn No longer placed on the EU market

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Withdrawn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European Union — CE/MDD Withdrawn

Specification

EUDAMED

Model / Reference: MONOART® CANNULA EM19 EM19 ASPIRATOR TIP EM19 ABSAUGKANÜLE, 22910XXX

Primary DI / UDI-DI: D-EM19ASPIRATORTIPTC
Basic UDI-DI: B-EM19ASPIRATORTIPTC
EMDN Code: Q019001 Saliva aspirators and saliva absorbents

Device Class: Class IIa
EU market of registration: Italy

Manufacturer details

EUDAMED SRN: IT-MF-000007762

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Properties

Other properties (11)

Sterile: No
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