77 results
·
22ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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21HK512D
FDA 510(k)
FDA Class 2
·Radiology
E-CUBE 9
FDA 510(k)
FDA Class 2
·Radiology
KYPHON XPANDER II INFLATABLE BONE TAMP
FDA 510(k)
FDA Class 2
·Orthopedic
KYPHOPAK TRAY
FDA Adverse Event
Malfunction
·MDT KYPHON NEUCHATEL MFG·Product code HRX·May 24, 2021
KYPHON XPANDER II INFLATABLE BONE TAMP
FDA Adverse Event
Malfunction
·MEDTRONIC MEXICO·Product code HRX·November 6, 2019
KYPHON XPANDER II INFLATABLE BONE TAMP
FDA Adverse Event
Malfunction
·MEDTRONIC MEXICO·Product code HRX·April 5, 2021
HEART LUNG MACHINE
FDA Adverse Event
Malfunction
·MAQUET CARDIOPULMONARY GMBH·Product code KFM·April 23, 2026
HEART LUNG MACHINE
FDA Adverse Event
Malfunction
·MAQUET CARDIOPULMONARY GMBH·Product code KFM·May 8, 2026
HEART LUNG MACHINE
FDA Adverse Event
Malfunction
·MAQUET CARDIOPULMONARY GMBH·Product code KFM·March 25, 2026
KYPHON XPANDER II INFLATABLE BONE TAMP
FDA Adverse Event
Malfunction
·MEDTRONIC MEXICO·Product code HRX·July 11, 2019
KYPHON XPANDER II INFLATABLE BONE TAMP
FDA Adverse Event
Malfunction
·MEDTRONIC MEXICO·Product code HRX·August 31, 2019
SYNERGY
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code LGW·October 1, 2008
CS300
FDA Adverse Event
Malfunction
·DATASCOPE CORP.·Product code DSP·July 29, 2011
MECHANICAL CHAIR/TRANSPORT CHAIR
FDA Adverse Event
JIANGSU YUYUE MEDICAL EQUIPMENT & SUPPLY CO., LTD·Product code INM·June 26, 2013
HEART LUNG MACHINE
FDA Adverse Event
Malfunction
·MAQUET CARDIOPULMONARY GMBH·Product code KFM·April 27, 2026
HEART LUNG MACHINE
FDA Adverse Event
Malfunction
·MAQUET CARDIOPULMONARY GMBH·Product code KFM·April 13, 2026
HEART LUNG MACHINE
FDA Adverse Event
Malfunction
·MAQUET CARDIOPULMONARY GMBH·Product code KFM·March 30, 2026
KYPHON XPANDER II INFLATABLE BONE TAMP
FDA Adverse Event
Malfunction
·MDT KYPHON NEUCHATEL MFG·Product code HRX·March 7, 2018
HEART LUNG MACHINE
FDA Adverse Event
Malfunction
·MAQUET CARDIOPULMONARY GMBH·Product code KFM·April 22, 2026
HEART LUNG MACHINE
FDA Adverse Event
Malfunction
·MAQUET CARDIOPULMONARY GMBH·Product code KFM·April 22, 2026