9 results
·
19ms
·
Sources: EU EUDAMED, US FDA
PO-200 BLOOD OXYGEN MONITOR
FDA 510(k)
FDA Class 2
·Anesthesiology
Brigade
FDA UDI
Nuvasive, Inc.·00887517672193·Brigade Trial, 18x34x36mm, 12°
LINER: MPACT FLAT PE HC LINER Ø36/E
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code LPH·March 14, 2022
PERMASHADE VENEER CEMENT
FDA 510(k)
FDA Class 2
·Dental
MPF ACETABULAR CUP
FDA 510(k)
FDA Class 2
·Orthopedic
*
FDA Adverse Event
Injury
·VASCOR MEDICAL·Product code DTB·June 1, 1999
FREESTYLE FLASH
FDA Adverse Event
Malfunction
·ABBOTT DIABETES CARE, INC., USA·Product code LFR·October 24, 2007
CONCERTO CRT-D DR
FDA Adverse Event
Malfunction
·MEDTRONIC MED REL, INC.·Product code NIK·October 31, 2012
FOOT CONTROL
FDA Adverse Event
Malfunction
·DEPUY SYNTHES POWER TOOLS·Product code HBC·October 11, 2013