257 results
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21ms
·
Sources: EU EUDAMED, US FDA
Acid, Hyaluronic, Intraarticular
FDA Pre-Market Approval
FDA Class 3
·TRIVISC
Acid, Hyaluronic, Intraarticular
FDA Pre-Market Approval
FDA Class 3
·TriVisc
Acid, Hyaluronic, Intraarticular
FDA Pre-Market Approval
FDA Class 3
·TriVisc
Acid, Hyaluronic, Intraarticular
FDA Pre-Market Approval
FDA Class 3
·TriVisc®
Fixed Awl
FDA UDI
SIGNATURE ORTHOPAEDICS PTY LTD·09348215066963·
ArcCHECK-MR
FDA 510(k)
FDA Class 2
·Radiology
Automated Insulin Dosing Device System, Single Hormonal Control
FDA Pre-Market Approval
FDA Class 3
·MiniMed 670G System
Sensor, Glucose, Invasive
FDA Pre-Market Approval
FDA Class 3
·Guardian Connect system
ADAPTA DR
FDA Adverse Event
Injury
·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code NVZ·October 10, 2014
AUTOLUBE-III
FDA Adverse Event
Malfunction
·DEPUY SYNTHES POWER TOOLS·Product code GEY·June 10, 2013
COLLEAGUE PRE P1.7
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·July 13, 2011
HEARTMATE MOBILE POWER UNIT, NA
FDA Adverse Event
Injury
·THORATEC CORPORATION·Product code DSQ·January 6, 2020
HEARTMATE MOBILE POWER UNIT, NA
FDA Adverse Event
Malfunction
·THORATEC CORPORATION·Product code DSQ·January 8, 2020
PATIENT CABLE
FDA Adverse Event
Malfunction
·THORATEC CORPORATION·Product code DSQ·September 8, 2020
HEARTMATE GOGEAR SHOWER BAG
FDA Adverse Event
Injury
·THORATEC CORPORATION·Product code DSQ·December 19, 2019
HEARTMATE MOBILE POWER UNIT, NA
FDA Adverse Event
Malfunction
·THORATEC CORPORATION·Product code DSQ·December 20, 2019
CONTOUR® NEXT
FDA Adverse Event
Malfunction
·ASCENSIA DIABETES CARE US INC.·Product code NBW·October 9, 2023
HEARTMATE SYSTEM MONITOR
FDA Adverse Event
Injury
·THORATEC CORPORATION·Product code DSQ·January 2, 2020
HEARTMATE MOBILE POWER UNIT, UK
FDA Adverse Event
Malfunction
·THORATEC CORPORATION·Product code DSQ·March 9, 2020
HEARTMATE MOBILE POWER UNIT, NA
FDA Adverse Event
Malfunction
·THORATEC CORPORATION·Product code DSQ·December 13, 2019