47 results · 28ms · Sources: EU EUDAMED, US FDA

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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