39 results
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25ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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SUPOLENE
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
Sklar®
FDA UDI
SKLAR CORPORATION·10649111288883·OP SCISS STR S/B 7 1/4"
UniTip Catheter
FDA UDI
Unisensor AG·07640172973868·
UniTip Catheter
FDA UDI
Unisensor AG·07640172973783·
KUSCHALL CHAMPION, KUSCHALL COMPACT, KUSCHALL ULTRA-LIGHT
FDA 510(k)
FDA Class 1
·Physical Medicine
TRITANIUM PERI-APATITIE ACETABULAR SOLID-BACKED SHELL, TRITANIUM PERI-APATITE
FDA 510(k)
FDA Class 2
·Orthopedic
STEM: QUADRA-H CEMENTLESS, HA COATED LAT STEM SIZE 3, SHORT NECK
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code JDI·April 13, 2021
PARADIGM REAL-TIME INSULIN INFUSION PUMP
FDA Adverse Event
Injury
·MEDTRONIC MINIMED·Product code OYC·June 3, 2013
UNKNOWN ZIMMER MIS TIBIAL COMPONENT
FDA Adverse Event
Injury
·ZIMMER INC.·Product code JWH·June 21, 2011
UNK
FDA Adverse Event
Injury
·PLAINFIELD-LOX-RX·Product code CAW·August 29, 2008
SUPERSHEATH
FDA Adverse Event
Malfunction
·TOGO MEDIKIT CO. LTD.·Product code DRE·December 2, 2016
SUPER SHEATH
FDA Adverse Event
Injury
·TOGO MEDIKIT CO., LTD.·Product code DRE·June 2, 2022
SUPERSHEATH
FDA Adverse Event
Injury
·TOGO MEDIKIT CO. LTD.·Product code DRE·August 12, 2018
SUPERSHEATH
FDA Adverse Event
Malfunction
·TOGO MEDIKIT CO. LTD.·Product code DRE·December 11, 2016
SUPER SHEATH
FDA Adverse Event
Injury
·TOGO MEDIKIT CO.LTD.·Product code DRE·January 18, 2018
SUPER SHEATH
FDA Adverse Event
Injury
·TOGO MEDIKIT CO., LTD.·Product code DRE·March 21, 2023
SUPER SHEATH
FDA Adverse Event
Injury
·TOGO MEDIKIT CO. LTD.·Product code DRE·April 28, 2020
SUPERSHEATH
FDA Adverse Event
Injury
·TOGO MEDIKIT CO. LTD.·Product code DRE·April 11, 2017
SUPER SHEATH
FDA Adverse Event
Injury
·TOGO MEDIKIT CO. LTD.·Product code DRE·February 11, 2020
SUPER SHEATH
FDA Adverse Event
Injury
·TOGO MEDIKIT CO., LTD.·Product code DRE·January 19, 2023