24 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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TRI-FIX SPINAL FIXATION SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
Zirlux
FDA UDI
HENRY SCHEIN, INC.·H65890109220·Zirlux Bite Ver Cyl Eng
Endo Carry-on Procedure Kit
FDA UDI
MEDIVATORS INC.·00677964152702·Endo Carry-on Procedure Kit contains Intercept ...
A NEW DAY
FDA UDI
FGX INTERNATIONAL INC.·00193033248720·
A NEW DAY
FDA UDI
FGX INTERNATIONAL INC.·00193033344149·
A NEW DAY
FDA UDI
FGX INTERNATIONAL INC.·00193033248713·
A NEW DAY
FDA UDI
FGX INTERNATIONAL INC.·00191905788749·
A NEW DAY
FDA UDI
FGX INTERNATIONAL INC.·00193033248706·
Matira
FDA UDI
Kalitec Direct LLC·B07307K0100220·Assembly, Caddie, 1-3L Plates, Hnged
Kalitec Special
FDA UDI
Kalitec Direct LLC·B073DRK0100220·SNII Awl Tap, 6.50mm
PROTON VISION
FDA 510(k)
FDA Class 2
·Radiology
DEPUY NEUFLEX PIP FINGER
FDA 510(k)
FDA Class 2
·Orthopedic
BD CONNECTA¿ STOPCOCKS CONNECTA PLUS
FDA Adverse Event
Malfunction
·BD INFUSION THERAPY SYSTEMS INC. S.A. DE C.V.·Product code FMG·July 12, 2018
BD VACUTAINER® SST¿ BLOOD COLLECTION TUBES
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO., (BD)·Product code JKA·May 9, 2019
BD VACUTAINER® SST¿ BLOOD COLLECTION TUBES
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO., (BD)·Product code JKA·May 16, 2019
DEXCOM G6 CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code QBJ·June 23, 2025
BD CONNECTA¿ STOPCOCK LEAKED
FDA Adverse Event
Malfunction
·BD INFUSION THERAPY SYSTEMS INC. S.A. DE C.V.·Product code FMG·October 16, 2018
9800
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·March 14, 2013
PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·August 14, 2014
TENDRIL SDX
FDA Adverse Event
Injury
·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code DTB·March 10, 2008