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Cannucce per L'esecuzione Del Test Del Respiro

by AB ANALITICA srl

Ref 15-26-100Model CANNUCCE PER L'ESECUZIONE DEL TEST DEL RESPIRO

Active European Union

CE MDR

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 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number803362278BBHTsc00000002ME Basic UDI-DI 08053303091864UDI-DIDate13 Aug 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  • Withdrawn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/MDR Active

Specification

EUDAMED

Device Name
Cannucce per L'esecuzione Del Test Del Respiro
Model / Reference
CANNUCCE PER L'ESECUZIONE DEL TEST DEL RESPIRO, 15-26-100
Primary DI / UDI-DI
08053303091864
Basic UDI-DI
803362278BBHTsc00000002ME
Direct Marketing DI
08053303091864
EMDN Code
V80 Clinical use accessories not included in other classes
Device Class
Class I
EU market of registration
Italy

Manufacturer details

EUDAMED SRN
IT-MF-000032625

Other devices from AB ANALITICA srl

See all devices from AB ANALITICA srl →

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