67 results · 21ms · Sources: EU EUDAMED, 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