524 results
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26ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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HWD Electrode Set
FDA UDI
Zoll Medical Corporation·00847946021986·PRO*PADZ HWD device (single kit)
HEX WRENCH DRIVER
FDA UDI
SNUCONE Co.,LTD.·08800020819048·
HEX WRENCH DRIVER
FDA UDI
SNUCONE Co.,LTD.·08800020819031·
Hospital Wearable Defibrillator
FDA UDI
ZOLL MANUFACTURING CORPORATION·00855778005159·
HOSPITAL WEARABLE DEFIBRILLATOR (HWD)
FDA Adverse Event
Injury
·ZOLL MANUFACTURING CORPORATION·Product code MVK·June 11, 2021
Hospital Wearable Defibrillator
FDA UDI
ZOLL MANUFACTURING CORPORATION·00855778005180·
Hospital Wearable Defibrillator
FDA UDI
ZOLL MANUFACTURING CORPORATION·00855778005173·
Hospital Wearable Defibrillator
FDA UDI
ZOLL MANUFACTURING CORPORATION·00855778005272·
Hospital Wearable Defibrillator
FDA UDI
ZOLL MANUFACTURING CORPORATION·00855778005203·
HWD
FDA Adverse Event
Malfunction
·ZOLL MANUFACTURING CORPORATION·Product code MVK·April 12, 2022
HWD
FDA Adverse Event
Malfunction
·ZOLL MANUFACTURING CORPORATION·Product code MVK·March 19, 2022
DEXCOM G5 MOBILE CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code PQF·January 4, 2018
HWD 1000 SYSTEM
FDA Adverse Event
Injury
·ZOLL MANUFACTURING CORPORATION·Product code MVK·September 11, 2024
HWD 1000 SYSTEM
FDA Adverse Event
Injury
·ZOLL MANUFACTURING CORPORATION·Product code MVK·June 8, 2022
HWD 1000 SYSTEM
FDA Adverse Event
Injury
·ZOLL MANUFACTURING CORPORATION·Product code MVK·August 28, 2023
HWD 1000 SYSTEM
FDA Adverse Event
Malfunction
·ZOLL MANUFACTURING CORPORATION·Product code MVK·May 29, 2024
HWD 1000 SYSTEM
FDA Adverse Event
Injury
·ZOLL MANUFACTURING CORPORATION·Product code MVK·August 4, 2022
HWD 1000 SYSTEM
FDA Adverse Event
Malfunction
·ZOLL MANUFACTURING CORPORATION·Product code MVK·February 16, 2023
HWD 1000 SYSTEM
FDA Adverse Event
Malfunction
·ZOLL MANUFACTURING CORPORATION·Product code MVK·February 16, 2023
HWD 1000 SYSTEM
FDA Adverse Event
Malfunction
·ZOLL MANUFACTURING CORPORATION·Product code MVK·February 16, 2023