174 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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3880 MRI Patient Monitoring System
FDA 510(k)
FDA Class 2
·Cardiovascular
PILLING
FDA UDI
TELEFLEX INCORPORATED·24026704513455·
Ophthalmic Retractor
FDA UDI
KATENA PRODUCTS, INC.·00841668100950·DESMARRES LID RETRACTOR #0
General Instruments
FDA UDI
ALPHATEC SPINE, INC.·00840180538746·SQUARE ENDPLATE SCRAPER, STRAIGHT
JOBST Elvarex
FDA UDI
BSN-Jobst GmbH·04019702384994·Elvarex Forte 3/Thigh High/Slant-Closed Toe-Ele...
JOBST Elvarex
FDA UDI
BSN-Jobst GmbH·04019702453478·ELVAREX 2/THIGH HIGH/OPEN TOE, E-VERSION, KNEE ...
KYMCO FORU, MODEL EQ10
FDA 510(k)
FDA Class 2
·Physical Medicine
HEITER 3000 HYPERTHERMIC PERFUSION SYSTEM
FDA 510(k)
FDA Class 2
·General Hospital
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