25 results
·
28ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
eNAT molecular collection and preservation medium
FDA 510(k)
FDA Class 2
·Microbiology
24M - Tampa Electric Co.
FDA UDI
Certified Safety Manufacturing, Inc.·00766588013497·24M Tampa Electric Co.
BICON DENTAL IMPLANT SYSTEM 3.0MM BICON DENTAL IMPLANT
FDA 510(k)
FDA Class 2
·Dental
TAGG DISPOSABLE VAGINAL SPECULUM
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
Widex
FDA UDI
Widex A/S·05706069728194·Widex EVOKE E-FS (Tan silk S-440 ) Telecoil, RC...
ALLEVYN LIFE SACRUM (LARGE) PACK OF 10
FDA Adverse Event
Injury
·SMITH & NEPHEW MEDICAL LTD.·Product code KGX·October 25, 2019
ALLEVYN LIFE SACRUM (LARGE) PACK OF 10
FDA Adverse Event
Injury
·SMITH & NEPHEW MEDICAL LTD.·Product code KGX·October 25, 2019
ALLEVYN LIFE SACRUM (LARGE) PACK OF 10
FDA Adverse Event
Injury
·SMITH & NEPHEW MEDICAL LTD.·Product code KGX·October 25, 2019
DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code QBJ·July 29, 2025
CONTOUR TEST STRIPS (50)
FDA Adverse Event
Injury
·BAYER HEALTHCARE, LLC·Product code NBW·October 15, 2008
ENDEAVOR SPRINT RX CORONARY STENT SYSTEM
FDA Adverse Event
Injury
·MEDTRONIC IRELAND·Product code NIQ·August 5, 2011
BRONCHIAL THERMOPLASTY CATHETER
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC - SAN JOSE·Product code OOY·July 2, 2013
TRELLIS-6 PERIPHERAL INFUSION SYSTEM
FDA Adverse Event
Injury
·MEDTRONIC COVIDIEN·Product code KRA·June 7, 2018
TRELLIS-6 PERIPHERAL INFUSION SYSTEM
FDA Adverse Event
Injury
·MEDTRONIC COVIDIEN·Product code KRA·June 7, 2018
VENA SEAL CLOSURE SYSTEM
FDA Adverse Event
Injury
·MEDTRONIC IRELAND·Product code PJQ·February 12, 2020
PROTEGE GPS SELF-EXPANDING BILIARY STENT SYSTEM 018
FDA Adverse Event
Injury
·MEDTRONIC COVIDIEN·Product code FGE·June 7, 2018
PROTEGE GPS SELF-EXPANDING BILIARY STENT SYSTEM 018
FDA Adverse Event
Injury
·MEDTRONIC COVIDIEN·Product code FGE·June 7, 2018
PROTEGE GPS SELF-EXPANDING BILIARY STENT SYSTEM 018
FDA Adverse Event
Injury
·MEDTRONIC COVIDIEN·Product code FGE·June 7, 2018
BLAKE DRAIN UNKNOWN PRODUCT
FDA Adverse Event
Injury
·ETHICON INC.·Product code GBX·January 5, 2022
HEARTMATE 3 LEFT VENTRICULAR ASSIST SYSTEM
FDA Adverse Event
Injury
·THORATEC CORPORATION·Product code DSQ·September 10, 2019