18 results
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24ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Endoskeleton TAS Plate
FDA 510(k)
FDA Class 2
·Orthopedic
MSI Precision Specialty Instruments
FDA UDI
Med Saver, Inc.·00194613017712·K-Wire, Double Ended, Trocar Point, Diameter Si...
MSI Precision Specialty Instruments
FDA UDI
Med Saver, Inc.·00194613017934·K-Wire, Double Ended, Trocar Point, Diameter Si...
Bernafon
FDA UDI
Bernafon AG·05711584087282·ZR1, KIT 312 NFM 85 R BE ZERENA 1
V200 VENTILATOR
FDA 510(k)
FDA Class 2
·Anesthesiology
MOXIE PLASTIC APPLICATOR AND MOXIE NON-APPLICATOR TAMPON
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
V200 / ESPRIT
FDA Adverse Event
Malfunction
·RESPIRONICS CALIFORNIA, LLC·Product code CBK·March 16, 2021
RESPIRONICS
FDA Adverse Event
Malfunction
·RESPIRONICS CALIFORNIA, LLC·Product code CBK·March 28, 2021
RESPIRONICS
FDA Adverse Event
Malfunction
·RESPIRONICS CALIFORNIA, LLC·Product code MNT·May 19, 2021
RESPIRONICS
FDA Adverse Event
Malfunction
·RESPIRONICS CALIFORNIA, LLC·Product code CBK·May 20, 2021
RESPIRONICS
FDA Adverse Event
Malfunction
·RESPIRONICS CALIFORNIA, LLC·Product code MNT·June 7, 2021
V200 VENTILATOR
FDA Adverse Event
Malfunction
·RESPIRONICS CALIFORNIA, INC·Product code CBK·December 9, 2020
RESPIRONICS
FDA Adverse Event
Malfunction
·RESPIRONICS CALIFORNIA, LLC·Product code MNT·June 21, 2021
QUICKFLEX MICRO LV LEAD
FDA Adverse Event
Malfunction
·ST. JUDE MEDICAL, INC., CRMD·Product code NIK·January 13, 2014
OT ULTRALINK METER
FDA Adverse Event
Malfunction
·LIFESCAN INC.·Product code NBW·August 4, 2011
EXCLAIM 8
FDA Adverse Event
Injury
·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·June 20, 2013
RELION INSULIN SYRINGES 1/2ML 31 GAUGE, 8MM (5/16") U-100 100COUNT
FDA Adverse Event
Malfunction
·BD MEDICAL - DIABETES CARE·Product code FMF·July 15, 2022
UNKNOWN SHOULDER COMPONENTS
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code HSD·November 1, 2023