179 results
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22ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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PerioLase Nd:YAG Pulsed Dental Laser System
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
Ophthalmic Retractor
FDA UDI
KATENA PRODUCTS, INC.·00841668100981·DESMARRES LID RETRACTOR #3
FULLY AUTOMATIC ELECTRONIC BLOOD PRESSURE MONITOR
FDA 510(k)
FDA Class 2
·Cardiovascular
CARDIVA CATALYST III SYSTEM WITH PROTAMINE SULFATE
FDA 510(k)
FDA Class 2
·Cardiovascular
SURDIAL X
FDA Adverse Event
Malfunction
·SHIBUYA (SBY)·Product code KDI·August 5, 2021
SURDIAL X
FDA Adverse Event
Malfunction
·SHIBUYA (SBY)·Product code KDI·August 5, 2021
SURDIAL X
FDA Adverse Event
Malfunction
·SHIBUYA (SBY)·Product code KDI·August 5, 2021
SURDIAL X
FDA Adverse Event
Malfunction
·SHIBUYA (SBY)·Product code KDI·August 5, 2021
SURDIAL X
FDA Adverse Event
Malfunction
·SHIBUYA (SBY)·Product code KDI·August 5, 2021
SURDIAL X
FDA Adverse Event
Malfunction
·SHIBUYA (SBY)·Product code KDI·August 5, 2021
SURDIAL X
FDA Adverse Event
Malfunction
·SHIBUYA (SBY)·Product code KDI·August 5, 2021
SURDIAL X
FDA Adverse Event
Malfunction
·SHIBUYA (SBY)·Product code KDI·August 5, 2021
SURDIAL X
FDA Adverse Event
Malfunction
·SHIBUYA (SBY)·Product code KDI·August 5, 2021
SURDIAL X
FDA Adverse Event
Malfunction
·SHIBUYA (SBY)·Product code KDI·August 5, 2021
NIPRO BLOOD TUBING SET W/TP
FDA Adverse Event
Malfunction
·NIPRO (THAILAND) CORP. LTD.·Product code FJK·February 6, 2024
ZILVER 635 SELF-EXPANDING BILIARY STENT
FDA Adverse Event
Injury
·COOK IRELAND LTD·Product code FGE·September 1, 2022
SURDIAL X
FDA Adverse Event
Malfunction
·SHIBUYA (SBY)·Product code KDI·August 5, 2021
ZILVER 635 SELF-EXPANDING BILIARY STENT
FDA Adverse Event
Injury
·COOK IRELAND LTD·Product code FGE·August 29, 2022
ZILVER 635 SELF-EXPANDING BILIARY STENT
FDA Adverse Event
Injury
·COOK IRELAND LTD·Product code FGE·August 26, 2022
SURDIAL X
FDA Adverse Event
Malfunction
·SHIBUYA (SBY)·Product code KDI·August 5, 2021