21 results
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29ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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MERI-DAPT(TM) HEMOSTASIS VALVE/TORQLOC TORQUE DEVI
FDA 510(k)
FDA Class 2
·Cardiovascular
ORTHOCOR ACTIVE DEVICE ORTHOCOR GENERAL USE ACTIVE DEVICE
FDA 510(k)
FDA Class 2
·Physical Medicine
CRYOBAG, MODEL CB
FDA 510(k)
FDA Unclassified
·Unknown
MICROTAINER SST GOLD
FDA Adverse Event
Malfunction
·BD CARIBE LTD.·Product code JKA·June 7, 2018
BD MICROTAINER® EDTA LAVENDAR TUBES
FDA Adverse Event
Malfunction
·BD CARIBE LTD.·Product code JKA·May 1, 2018
BD MICROTAINER® EDTA LAVENDAR TUBES
FDA Adverse Event
Malfunction
·BD CARIBE LTD.·Product code JKA·May 16, 2018
MICROTAINER SST GOLD
FDA Adverse Event
Malfunction
·BECTON DICKINSON CARIBE LTD·Product code JKA·May 7, 2018
BD MICROTAINER® EDTA LAVENDER TUBES
FDA Adverse Event
Malfunction
·BD CARIBE LTD.·Product code JKA·April 27, 2018
BD MICROTAINER® EDTA LAVENDAR TUBES
FDA Adverse Event
Malfunction
·BD CARIBE LTD.·Product code JKA·May 3, 2018
BD MICROTAINER® BLOOD COLLECTION TUBES
FDA Adverse Event
Malfunction
·BD CARIBE LTD.·Product code JKA·December 3, 2017
SPRINT QUATTRO SECURE
FDA Adverse Event
Injury
·MEDTRONIC PUERTO RICO, INC.·Product code LWS·December 13, 2010
PUMP IN STYLE ADVANCED BREAST PUMP GO TOTE
FDA Adverse Event
Injury
·MEDELA, INC.·Product code HGX·January 15, 2013
ENDOTAK RELIANCE
FDA Adverse Event
Injury
·CPI - DEL CARIBE·Product code LWS·July 9, 2014
PENTAX
FDA Adverse Event
Injury
·PENTAX·Product code EOQ·January 10, 2017
PENTAX
FDA Adverse Event
Injury
·PENTAX·Product code EOQ·January 10, 2017
PENTAX
FDA Adverse Event
Injury
·PENTAX·Product code EOQ·January 10, 2017
PENTAX
FDA Adverse Event
Injury
·PENTAX·Product code EOQ·January 10, 2017
PENTAX
FDA Adverse Event
Injury
·PENTAX·Product code EOQ·January 10, 2017
PENTAX
FDA Adverse Event
Injury
·PENTAX·Product code EOQ·January 10, 2017
PENTAX
FDA Adverse Event
Injury
·PENTAX·Product code EOQ·January 10, 2017