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bioXtra Dry Mouth Oral Gel

by Lifestream Pharma N.V. 2 variants

Ref 90077419Model bioXtra Dry Mouth Oral Gel 40ml

Active European Union

CE MDR

Valid until

3 Oct 2028

CE MDR certificate

FDA recalls

Not applicable

No FDA record for this device

Documents

1 certificate

Certifier SGS Belgium NV

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR NumberBE23/00000293 Date25 Nov 2025IssuedStatusActive expires 3 Oct 2028

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)
  • BE23/00000293 Active Supplemented

    Quality management system EU MDR

    Certifier
    SGS Belgium NV 1639
    Issued
    25 Nov 2025
    Expires
    3 Oct 2028
    Reason
    Other

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
bioXtra Dry Mouth
Model / Reference
bioXtra Dry Mouth Oral Gel 40ml, 90077419
Primary DI / UDI-DI
05425005127623
Basic UDI-DI
542500512BXOG01YF
EMDN Code
V9017 Oral administration preparations not included in other classes
Device Class
Class IIa
EU market of registration
Czechia

Manufacturer details

EUDAMED SRN
BE-MF-000001909

Other devices from Lifestream Pharma N.V.

See all devices from Lifestream Pharma N.V. →

Properties

Other properties (13)

  • Sterile: No
  • Implantable: No
  • Reusable: No
  • Contains Latex: 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