39 results
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27ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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LINA XCISE MODEL MOR-1515
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
GPAC II KNEE SYSTEM
FDA UDI
Biomet Orthopedics, LLC·00880304184688·
Oticon
FDA UDI
Oticon A/S·05707131164629·K13, BTE 13 SIL
UniTip Catheter
FDA UDI
Unisensor AG·07640172971239·
SYNCHRON CONTROL
FDA 510(k)
FDA Class 1
·Clinical Chemistry
SYNTHES STRAIGHT WRIST FUSION PLATE, 170MM
FDA 510(k)
FDA Class 2
·Orthopedic
BALL HEADS: MECTACER BIOLOX DELTA CERAMIC 12/14 Ø 28 SIZE L
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code LZO·December 14, 2021
MPACT DM DOUBLE MOBILITY HC LINER Ø 50/28
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code MEH·July 30, 2019
LINER: MPACT DM DOUBLE MOBILITY HC LINER 22.2/DMC
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code MEH·December 7, 2020
9900
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·May 2, 2013
NATURALYTE
FDA Adverse Event
Death
·FRESENIUS MEDICAL CARE NORTH AMERICA·Product code KPO·September 3, 2014
COLLEAGUE PRE P1.7
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·May 25, 2011
LINER: MPACT DM DM CONVERTER TIN COATED D/DMB
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code LZO·June 27, 2024
CANTATA DUO 2.8 SUPERSELECTIVE MICROCATHETER
FDA Adverse Event
Malfunction
·COOK INC·Product code KRA·August 14, 2017
STEM: M-VIZION PROXIMAL BODY Ø20MM L 90MM STD
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code LZO·April 9, 2024
CANTATA 2.8 SUPERSELECTIVE MICROCATHETER
FDA Adverse Event
Injury
·COOK INC·Product code KRA·November 17, 2017
CANTATA 2.5 SUPERSELECTIVE MICROCATHETER
FDA Adverse Event
Malfunction
·COOK INC·Product code KRA·September 17, 2018
CANTATA DUO 2.8 SUPERSELECTIVE MICROCATHETER
FDA Adverse Event
Malfunction
·COOK INC·Product code KRA·September 11, 2018
CANTATA 2.5 SUPERSELECTIVE MICROCATHETER
FDA Adverse Event
Injury
·COOK INC·Product code KRA·July 28, 2017
CANTATA DUO 2.8 SUPERSELECTIVE MICROCATHETER
FDA Adverse Event
Malfunction
·COOK INC·Product code KRA·June 15, 2017