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Spiro Handle

Bionet CO,LTD · Model Spiro Handle · UDI-DI 08809276943729

BZG
1
510(k) clearances
31
Adverse events
1
Recalls
93
Facilities

Description

SPIROMETER, DIAGNOSTIC

Recalls

DateFirmReason
2024-10-11Baxter Healthcare CorporationThere is the potential for exam files being assigned duplicate Unique Identifiers (UIDs),. If the system receiving the DICOM file (e.g., Picture Archiving and Communication System

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.