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Kit Para Sibo/Intolerancias Azucares Lactosa

by Ayala Sample Kits, S.L.

Ref CAL018.4Model 7ATFRU, 7ATLAC, 7ATSAC, 7SIBOGLU, 7SIBOLOL, 7ATSOR, 8ATFRU, 8ATLAC, 8ATSAC, 8SIBOGLU, 8SIBOLSA, 8SIBOLOL, 8ATGAL, 8ATSOR, 8ATXOL, S8ATFRU, S8SIBOGLU, S8ATXIL, ATFRU, ATFRSO, ATGAL, ATLAC, ATSAC, SIBOGLU, SIBOLOL, SIBOLSA, CAL016.1-3, CAL018.1-10, etc

Active European Union

CE IVDR

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None, self-declared

Class I: no certifier involved

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/IVDR Number8437026387AIRTESTT8 Basic UDI-DI 08436628290301UDI-DIDate17 Jun 2026RegisteredStatusActive

Certificates

0 certificates · EUDAMED

No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/IVDR Active

Specification

EUDAMED

Device Name
Kit Airtest
Model / Reference
7ATFRU, 7ATLAC, 7ATSAC, 7SIBOGLU, 7SIBOLOL, 7ATSOR, 8ATFRU, 8ATLAC, 8ATSAC, 8SIBOGLU, 8SIBOLSA, 8SIBOLOL, 8ATGAL, 8ATSOR, 8ATXOL, S8ATFRU, S8SIBOGLU, S8ATXIL, ATFRU, ATFRSO, ATGAL, ATLAC, ATSAC, SIBOGLU, SIBOLOL, SIBOLSA, CAL016.1-3, CAL018.1-10, etc, CAL018.4
Primary DI / UDI-DI
08436628290301
Basic UDI-DI
8437026387AIRTESTT8
EMDN Code
W05019099 Samples collection devices - other
Device Class
Class A
EU market of registration
Spain

Manufacturer details

EUDAMED SRN
ES-MF-000037853

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Properties

  • Professional Testing

Other properties (10)

  • Sterile: No
  • Human Tissues: No
  • Animal Tissues: No
  • Microbial Substances: No
  • Reagent: No
  • Self Testing: No
  • Near-Patient Testing: No
  • Companion Diagnostics: No
  • Surgical Instrument: No
  • New Device: No