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Posterior Mouthpiece

by Zyris, Inc. 4 variants

Ref AIL0250-GRCModel Posterior MP, Customer Success Kit, GRC

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 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-00810032661618 Basic UDI-DI 00810032661618UDI-DIDate5 Mar 2026RegisteredStatusActive

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

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDD Active

Specification

EUDAMED

Model / Reference
Posterior MP, Customer Success Kit, GRC, AIL0250-GRC
Primary DI / UDI-DI
00810032661618
Basic UDI-DI
B-00810032661618
EMDN Code
Q019001 Saliva aspirators and saliva absorbents
Device Class
Class IIa
EU market of registration
Greece

Manufacturer details

EUDAMED SRN
US-MF-000034843
Authorised representative
Emergo Europe B.V. NL-AR-000000116

Other devices from Zyris, Inc.

See all devices from Zyris, Inc. →

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