328 results
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25ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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MEMORY PUMP MODEL Y4947
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
EVONOS
FDA UDI
Gyrus ACMI, LLC·00821925018556·CUPPED FORCEPS CURVED UP
SYNGO AORTIC VALVEGUIDE SOFTWARE
FDA 510(k)
FDA Class 2
·Radiology
DATEX-OHMEDA TEC 7 ANESTHESIA VAPORIZER (ENFLURANE)
FDA 510(k)
FDA Class 2
·Anesthesiology
PENTAX
FDA Adverse Event
Injury
·PENTAX·Product code EOQ·January 10, 2017
PENTAX
FDA Adverse Event
Injury
·PENTAX·Product code EOQ·January 10, 2017
PENTAX
FDA Adverse Event
Injury
·PENTAX·Product code EOQ·January 10, 2017
PENTAX
FDA Adverse Event
Injury
·PENTAX·Product code EOQ·January 10, 2017
PENTAX
FDA Adverse Event
Injury
·PENTAX·Product code EOQ·January 10, 2017
PENTAX
FDA Adverse Event
Injury
·PENTAX·Product code EOQ·January 10, 2017
PENTAX
FDA Adverse Event
Injury
·PENTAX·Product code EOQ·January 10, 2017
PENTAX
FDA Adverse Event
Injury
·PENTAX·Product code EOQ·January 10, 2017
PENTAX
FDA Adverse Event
Malfunction
·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FAJ·December 27, 2021
FEMTO LDV SYSTEM
FDA Adverse Event
Injury
·SIE AG, SURGICAL INSTRUMENT ENGINEERING·Product code GEX·May 20, 2013
INSYNC SENTRY
FDA Adverse Event
Injury
·MEDTRONIC S.A.·Product code NIK·June 16, 2011
PERCLOSE PROGLIDE 6F SUTURE MEDIATED CLOSURE (SMC) SYSTEM
FDA Adverse Event
Injury
·ABBOTT VASCULAR REDWOOD CITY·Product code MGB·August 21, 2008
PENTAX
FDA Adverse Event
Malfunction
·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FAJ·October 15, 2021
PENTAX
FDA Adverse Event
Malfunction
·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FAJ·June 17, 2022
PENTAX
FDA Adverse Event
Malfunction
·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FAJ·December 27, 2021
PENTAX
FDA Adverse Event
Malfunction
·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FAJ·December 8, 2021