47 results
·
28ms
·
Sources: EU EUDAMED, US FDA
TEMPUS IC PROFESSIONAL PATIENT MONITOR
FDA 510(k)
FDA Class 2
·Cardiovascular
Portex
FDA UDI
ICU MEDICAL, INC.·15019517075779·
MaxFuse VBR, 10 (D) x 12 (W) x 38 (H)
FDA UDI
Pioneer Surgical Technology, Inc.·00846468055301·
MESH URETERAL STENT
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
EAGLE ENDO SPECIMEN RETRIEVAL BAG
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
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
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
VASO VIEW HEMOPRO
FDA Adverse Event
Malfunction
·MAQUET CARDIOVASCULAR LLC·Product code GEI·April 8, 2019
KYPHON XPANDER II INFLATABLE BONE TAMP
FDA Adverse Event
Malfunction
·MDT KYPHON NEUCHATEL MFG·Product code HRX·March 7, 2018
QUADRA ASSURA CRT-D, DF4 CONNECTOR
FDA Adverse Event
Malfunction
·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NIK·May 9, 2013
SWAN-GANZ CATHETER
FDA Adverse Event
Malfunction
·EDWARDS LIFESCIENCES, PR·Product code DYG·May 24, 2011
SELOX SR 45
FDA Adverse Event
Injury
·BIOTRONIK, GMBH AND CO.·Product code DTB·August 5, 2008
KYPHON XPANDER II INFLATABLE BONE TAMP
FDA Adverse Event
Malfunction
·MEDTRONIC SOFAMOR DANEK·Product code HRX·May 17, 2018
1030489-2019-01511
FDA Adverse Event
Death
·MEDTRONIC SOFAMOR DANEK USA, INC.·Product code NDN·December 31, 2019
KYPHON XPANDER
FDA Adverse Event
Malfunction
·MEDTRONIC MEXICO·Product code HRX·March 23, 2021
KYPHON XPANDER¿ II INFLATABLE BONE TAMP
FDA Adverse Event
Malfunction
·MEDTRONIC MEXICO S. DE R.L. DE CV·Product code HRX·August 26, 2025
KYPHON XPANDER
FDA Adverse Event
Malfunction
·MEDTRONIC MEXICO·Product code HRX·April 15, 2019