19 results
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21ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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2.5MM TURBO ELITE 035, 2.3MM TURBO ELITE 035
FDA 510(k)
FDA Class 2
·Cardiovascular
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172970782·
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172971192·
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172973264·
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172970751·
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172970775·
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172970768·
AMSCO V-PRO 1 LOW/PLUS/MAX TEMPERATURE STERILIZATION SYSTEM
FDA 510(k)
FDA Class 2
·General Hospital
DP-5 DIGITAL ULTRASONIC DIAGNOSTIC IMAGING SYSTEM DP-7 DIGITAL ULTRASONIC DIAGNOSTIC IMAGING SYSTEM
FDA 510(k)
FDA Class 2
·Radiology
INION OTPS BIOABSOBABLE FREEDOMPLATE
FDA Adverse Event
Injury
·INION OY·Product code HRS·November 18, 2014
INION OTPS BIOABSOBABLE FREEDOMPLATE
FDA Adverse Event
Injury
·INION OY·Product code HRS·May 14, 2015
INION OTPS BIOABSORBABLE FREEDOMPLATE
FDA Adverse Event
Injury
·INION OY·Product code HRS·March 19, 2015
HICKMAN TRIFUSION 19CM STRAIGHT KIT WITH INTERMEDIATE KIT
FDA Adverse Event
Malfunction
·C. R. BARD INC. (BASD)·Product code LJS·May 15, 2013
PARADIGM REAL-TIME INSULIN INFUSION PUMP
FDA Adverse Event
Malfunction
·MEDTRONIC MINIMED·Product code OYC·September 26, 2014
MAGELLAN BC 21G X 1.25"
FDA Adverse Event
Malfunction
·COVIDIEN·Product code FMI·June 10, 2011
LASSOSTARNAV,10P,15MM DIA LOOP
FDA Adverse Event
Injury
·BIOSENSE WEBSTER INC·Product code DRF·February 22, 2023
LASSOSTAR CATHETER
FDA Adverse Event
Death
·BIOSENSE WEBSTER INC.·Product code DRF·December 30, 2020
LASSOSTAR NAV CIRCULAR MAPPING CATHETER
FDA Adverse Event
Malfunction
·BIOSENSE WEBSTER INC·Product code DRF·November 23, 2022
INION OTPS BIOABSORBABLE FREEDOMPLATE
FDA Adverse Event
Injury
·INION OY·Product code HRS·June 5, 2015