17 results
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40ms
·
Sources: EU EUDAMED, US FDA
Pulmonx Corp
Manufacturer
🇺🇸 United States·1 Basic UDI-DI·2 Devices·1 Importer
PULMONX, Corp.
FDA registration
PULMONX, Corp.·5 products·🇺🇸 United States
Chartis Pulmonary Assessment Catheter XL
Device
EU MDR
·
Eu Md Class 2a
·Pulmonx Corp·On the market·18 countries
Chartis Pulmonary Assessment System Catheter
Device
EU MDR
·
Eu Md Class 2a
·Pulmonx Corp·On the market·18 countries
Chartis Catheter
Basic UDI-DI
EU MDR
·
Eu Md Class 2a
·Pulmonx Corp·2 devices
ZEPHYR ENDOBRONCHIAL VALVE SYSTEM
FDA Adverse Event
Malfunction
·PULMONX CORP.·Product code NJK·September 22, 2025
ZEPHYR ENDOBRONCHIAL VALVE
FDA Adverse Event
Malfunction
·PULMONX, CORP·Product code NJK·August 6, 2025
ZEPHYR ENDOBRONCHIAL VALVE
FDA Adverse Event
Injury
·PULMONX, CORP.·Product code NJK·April 28, 2025
ZEPHYR ENDOBRONCHIAL VALVE
FDA Adverse Event
Malfunction
·PULMONX CORP.·Product code NJK·May 19, 2025
ZEPHYR
FDA Adverse Event
Injury
·PULMONX, CORP.·Product code NJK·January 12, 2022
Zephyr Endobronchial Valve (EBV) 5.5-LP, REF: EBV-TS-5.5-LP
FDA Recall
Open, Classified
·Pulmonx, Corp.·Product code NJK·August 31, 2023
Zephyr Endobronchial Valve (EBV) 5.5-LP, REF: EBV-TS-5.5-LP
FDA Enforcement
Class II
·Ongoing·Pulmonx, Corp.·November 15, 2023
UNKNOWN EMPRINT ANTENNA
FDA Adverse Event
Injury
·COVIDIEN LP - SUPERDIMENSION INC·Product code NEY·August 18, 2021
Pulmonx GmbH
Authorized representative
🇩🇪 Germany·1 Manufacturer·2 Devices
Pulmonx GmbH
Importer
🇩🇪 Germany·1 Manufacturer
PULMONEX XENON SYSTEM
FDA Adverse Event
Injury
·BIODEX MEDICAL SYSTEMS, INC.·Product code IYT·September 22, 1998
PULMONOX II
FDA Adverse Event
Injury
·PULMONOX MEDICAL CORP.·Product code MRP·February 12, 1997