67 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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SonoSite iViz Ultrasound System
FDA 510(k)
FDA Class 2
·Radiology
Bernafon
FDA UDI
Bernafon AG·05711584075555·ZR9 MNR, 2.4G NFM PB SABE/MAC ZERENA 9
RESTORIS
FDA UDI
MAKO SURGICAL CORP.·00848486000905·MCK Onlay Tibial Insert
RESTORIS
FDA UDI
MAKO SURGICAL CORP.·00848486002220·MCK Onlay Tibial Insert
RESTORIS
FDA UDI
MAKO SURGICAL CORP.·00848486002251·MCK Onlay Tibial Insert
RESTORIS
FDA UDI
MAKO SURGICAL CORP.·00848486000882·MCK Onlay Tibial Insert
RESTORIS
FDA UDI
MAKO SURGICAL CORP.·00848486002244·MCK Onlay Tibial Insert
RESTORIS
FDA UDI
MAKO SURGICAL CORP.·00848486002237·MCK Onlay Tibial Insert
RESTORIS
FDA UDI
MAKO SURGICAL CORP.·00848486002268·MCK Onlay Tibial Insert
RESTORIS
FDA UDI
MAKO SURGICAL CORP.·00848486000998·MCK Onlay Tibial Insert
RESTORIS
FDA UDI
MAKO SURGICAL CORP.·00848486002275·MCK Onlay Tibial Insert
LOW FLUID ALARM
FDA 510(k)
FDA Class 2
·General Hospital
ACCU-CHEK FLEXLINK PLUS INFUSION SET, ACCU-CHECK LINKASSIST PLUS INSERTION DEVICE
FDA 510(k)
FDA Class 2
·General Hospital
KYPHX HV-R BONE CEMENT
FDA Adverse Event
Malfunction
·MDT KYPHON NEUCHATEL MFG·Product code NDN·May 29, 2019
KYPHON HV-R BONE CEMENT
FDA Adverse Event
Malfunction
·MDT KYPHON NEUCHATEL MFG·Product code NDN·April 29, 2019
KYPHON HV-R BONE CEMENT
FDA Adverse Event
Malfunction
·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NDN·June 6, 2019
MENICON ASRB (ASMOFILCON A) SILICONE HYDROGEL SOFT CONTACT LENS
FDA Adverse Event
Injury
·MENICON CO., LTD.·Product code LPL·March 18, 2026
KYPHON HV-R BONE CEMENT
FDA Adverse Event
Malfunction
·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NDN·September 20, 2019
KYPHON HV-R BONE CEMENT
FDA Adverse Event
Malfunction
·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NDN·July 15, 2019
KYPHON HV-R BONE CEMENT
FDA Adverse Event
Malfunction
·MEDTRONIC MEXICO·Product code NDN·March 25, 2020