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Disbiosi Intestinale

by Micro Trace Diagnostici SRL

Ref MTR 7032, MTR 7032/Q

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 Number805699925MTRPRELURILW Basic UDI-DI Date10 Apr 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  • Withdrawn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
Sistema di raccolta campioni di urine per invio e analisi in laboratorio
Model / Reference
MTR 7032, MTR 7032/Q
Primary DI / UDI-DI
08056999250386, 08056999250607
Basic UDI-DI
805699925MTRPRELURILW
EMDN Code
W05010202 Urine collection, tubes
Device Class
Class A
EU market of registration
Italy
Sweden

Manufacturer details

EUDAMED SRN
IT-MF-000033799

From the manufacturer

Manufacturer's product page: Disbiosi intestinale

Other devices from Micro Trace Diagnostici SRL

See all devices from Micro Trace Diagnostici SRL →

Properties

  • Near-Patient Testing

Other properties (10)

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