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HVE suction tubes

by Premium Plus International Limited 8 variants

Ref 005LASS

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

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-+D838005LASS4 Basic UDI-DI +D838005LASS4UDI-DIDate27 May 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  • Withdrawn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

Device Name
Dental Suction Tips
Model / Reference
005LASS
Primary DI / UDI-DI
+D838005LASS4
Basic UDI-DI
B-+D838005LASS4
EMDN Code
Q019001 Saliva aspirators and saliva absorbents
Device Class
Class IIa
EU market of registration
Poland

Manufacturer details

EUDAMED SRN
HK-MF-000039905
Authorised representative
Premium Plus Poland sp. z o.o. PL-AR-000030110

Other devices from Premium Plus International Limited

See all devices from Premium Plus International Limited →

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