38 results
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31ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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KIMGUARD ONE-STEP STERILIZATION WRAP
FDA 510(k)
FDA Class 2
·General Hospital
MAGNUM INSTRUMENTATION
FDA UDI
Biomet Uk Ltd·05019279440313·
M2a-Magnum™
FDA UDI
Biomet Orthopedics, LLC·00887868474316·
BD VACUTAINER TRACE ELEMENT SERUM PLUS TUBE AND BD VACUTAINER TRACE ELEMENT K2EDTA PLUS TUBE, MODELS 368380/368381
FDA 510(k)
FDA Class 2
·Clinical Chemistry
STAXX IBL SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
Widex
FDA UDI
Widex A/S·05706069812541·Widex EVOKE E-PA (Cappuccino brown ) 440, RC coil
6.0MM/10.0MM STEPPED DRILL BITCANNULATED/LARGE QC/435MM
FDA Adverse Event
Malfunction
·SYNTHES MONUMENT·Product code HTO·May 24, 2016
PARADIGM INSULIN INFUSION PUMP
FDA Adverse Event
Injury
·MEDTRONIC MINIMED·Product code LZG·June 3, 2013
COAGUCHEK ® XS SYSTEM
FDA Adverse Event
Injury
·ROCHE DIAGNOSTICS·Product code GJS·June 27, 2011
ZENITH AAA ENDOVASCULAR GRAFT ILIAC LEG
FDA Adverse Event
Injury
·COOK INC.·Product code MIH·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