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TransAir3
Medi Soft SA · Model TransAir3 · UDI-DI 05407003162011
1
510(k) clearances
67
Adverse events
5
Recalls
33
Facilities
Description
Pulmonary Function Testing Device, intended for measuring lung volumes by spirometry and Helium dilution
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2024-04-08 | Vyaire Medical, Inc. | Potential of the nozzle separating during patient use. |
| 2016-05-13 | Innovision A/S | The purpose of the recall is to replace data transmission cable (USB-cable) connecting the lnnocor device with an external computer. The replacement USB cable will provide galvani |
| 2009-11-19 | Philips Healthcare Inc. | Power cords' prongs may crack or fail -- Philips was notified that FDA is investigating whether certain types of Electri-Cord Manufacturing Company power cords used with medical de |
| 2009-11-19 | Philips Healthcare Inc. | Power cords' prongs may crack or fail -- Philips was notified that FDA is investigating whether certain types of Electri-Cord Manufacturing Company power cords used with medical de |
| 2009-11-19 | Philips Healthcare Inc. | Power cords' prongs may crack or fail -- Philips was notified that FDA is investigating whether certain types of Electri-Cord Manufacturing Company power cords used with medical de |
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Get your free API keyRead the docsData 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.