26 results
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20ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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RETROFLEX 3 INTRODUCER SHEATH SET, MODELS 9120S23 AND 9120S26
FDA 510(k)
FDA Class 2
·Cardiovascular
UNKNOWN EDWARDS TRANSFEMORAL SHEATH
FDA Adverse Event
Injury
·EDWARDS LIFESCIENCES·Product code DYB·March 12, 2026
ESHEATH INTRODUCER SHEATH
FDA Adverse Event
Injury
·EDWARDS LIFESCIENCES·Product code DYB·December 17, 2021
UNKNOWN EDWARDS TRANSFEMORAL SHEATH
FDA Adverse Event
Injury
·EDWARDS LIFESCIENCES·Product code NPT·November 18, 2020
UNKNOWN EDWARDS TRANSFEMORAL SHEATH
FDA Adverse Event
Injury
·EDWARDS LIFESCIENCES·Product code NPT·November 21, 2020
EDWARDS TRANSCATHETER TF SHEATH
FDA Adverse Event
Injury
·EDWARDS LIFESCIENCES·Product code NPT·November 20, 2018
UNKNOWN EDWARDS TRANSFEMORAL SHEATH
FDA Adverse Event
Injury
·EDWARDS LIFESCIENCES·Product code NPT·November 25, 2020
UNKNOWN EDWARDS TRANSFEMORAL SHEATH
FDA Adverse Event
Injury
·EDWARDS LIFESCIENCES·Product code NPT·November 21, 2020
UNKNOWN EDWARDS LIFESCIENCES SHEATH
FDA Adverse Event
Injury
·EDWARDS LIFESCIENCES·Product code DYB·May 30, 2024
EDWARDS TRANSCATHETER ESHEATH
FDA Adverse Event
Injury
·EDWARDS LIFESCIENCES·Product code NPU·November 20, 2018
EDWARDS SAPIEN 3 TRANSCATHETER HEART VALVE
FDA Adverse Event
Injury
·EDWARDS LIFESCIENCES LLC·Product code NPT·December 5, 2024
UNKNOWN EDWARDS SHEATH
FDA Adverse Event
Injury
·EDWARDS LIFESCIENCES·Product code NPT·November 15, 2019
UNKNOWN EDWARDS SHEATH
FDA Adverse Event
Injury
·EDWARDS LIFESCIENCES·Product code NPT·November 21, 2019
UNKNOWN EDWARDS SHEATH
FDA Adverse Event
Injury
·EDWARDS LIFESCIENCES·Product code NPT·November 15, 2019
UNKNOWN EDWARDS TRANSFEMORAL SHEATH
FDA Adverse Event
Injury
·EDWARDS LIFESCIENCES·Product code NPT·December 17, 2019
UNKNOWN EDWARDS TRANSFEMORAL SHEATH
FDA Adverse Event
Injury
·EDWARDS LIFESCIENCES·Product code NPT·December 17, 2019
MAR COR SERVICES SEMPER PURE RO MACHINE
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
CODMAN SLIM-LOC SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
FOOTPRINT ULTRA PK SUTURE ANCHOR, 4.5
FDA Adverse Event
Injury
·SMITH & NEPHEW, INC.·Product code MBI·August 4, 2015
FOOTPRINT ULTRA PK SUTURE ANCHOR, 4.5
FDA Adverse Event
Injury
·SMITH & NEPHEW, INC.·Product code MBI·July 28, 2015