3,007 results
·
39ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
Ultra PC % Flowmeter, PEU Model
FDA UDI
ACCUTRON, INC.·00813830025392·Medical gas mixer
Ultra PC % Package E, PEU
FDA UDI
ACCUTRON, INC.·00813830025484·
Ultra PC % Package B, PEU Model
FDA UDI
ACCUTRON, INC.·00813830026252·
Ultra PC % Package C, PEU
FDA UDI
ACCUTRON, INC.·00813830025422·
Ultra PC % Package D, PEU
FDA UDI
ACCUTRON, INC.·00813830025453·
Ultra PC % Package F, PEU
FDA UDI
ACCUTRON, INC.·00813830025514·
PowerCordEU
FDA UDI
CAMBRIDGE INTERVENTIONAL LLC·00811746030721·CRF Power Cord
Permablate
FDA UDI
GMMI SDN. BHD.·00860004198826·Permablate Electrolysis Unit
PEU Scavenging Circuit I
FDA UDI
ACCUTRON, INC.·00813830025194·
PEU Scavenging Ciruit II
FDA UDI
ACCUTRON, INC.·00813830021349·
HF SENSOR DELIVERY SYSTEM
FDA Adverse Event
Injury
·ST. JUDE MEDICAL, INC. - CARDIOMEMS·Product code MOM·March 11, 2016
HF SENSOR DELIVERY SYSTEM
FDA Adverse Event
Injury
·ST. JUDE MEDICAL, INC. - CARDIOMEMS·Product code MOM·May 18, 2016
POWER CORD 110V
FDA Adverse Event
Malfunction
·ST. JUDE MEDICAL, INC.·Product code MOM·December 1, 2021
CARDIOMEMS POWER SUPPLY
FDA Adverse Event
Malfunction
·ST. JUDE MEDICAL, INC. - CARDIOMEMS·Product code MOM·February 22, 2022
CARDIOMEMS POWER SUPPLY
FDA Adverse Event
Malfunction
·ST. JUDE MEDICAL, INC.·Product code MOM·February 2, 2022
CARDIOMEMS PATIENT ELECTRONIC SYSTEM
FDA Adverse Event
Injury
·ST. JUDE MEDICAL, INC.·Product code MOM·July 25, 2023
CARDIOMEMS PATIENT ELECTRONIC SYSTEM
FDA Adverse Event
Malfunction
·ST. JUDE MEDICAL, INC.·Product code MOM·March 12, 2024
CARDIOMEMS PATIENT ELECTRONIC SYSTEM
FDA Adverse Event
Injury
·ST. JUDE MEDICAL, INC.·Product code MOM·July 28, 2023
CARDIOMEMS PATIENT ELECTRONIC SYSTEM
FDA Adverse Event
Malfunction
·ST. JUDE MEDICAL, INC.·Product code MOM·October 18, 2021
HF SENSOR DELIVERY SYSTEM
FDA Adverse Event
Injury
·ST. JUDE MEDICAL, INC. - CARDIOMEMS·Product code MOM·May 29, 2019