442 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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ACTIVE INTACT PTH ELISA
FDA 510(k)
FDA Class 2
·Clinical Chemistry
21.3-INCH(54 CM) MONOCHROME LCD MONITOR MDL2115A (ME353I), (DV3MM-HB), (ME353IM)
FDA 510(k)
FDA Class 2
·Radiology
RejuvatoneMD
FDA 510(k)
FDA Class 2
·Neurology
AE-QAS-K521-99
FDA Adverse Event
Injury
·AESCULAP AG·Product code JWH·April 22, 2026
AE-QAS-K521-99
FDA Adverse Event
Injury
·AESCULAP AG·Product code JWH·April 22, 2026
TRANSTAR STRETCHER
FDA Adverse Event
Malfunction
·HILLROM DE MEXICO S DE RL DE CV·Product code FPO·May 13, 2014
MEDTRONIC.SIGMA
FDA Adverse Event
Injury
·IPG MFG SWITZERLAND·Product code NVZ·February 9, 2013
9600
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·January 4, 2011
PENTAX
FDA Adverse Event
Malfunction
·Product code CAL·July 21, 2021
PENTAX
FDA Adverse Event
Malfunction
·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code EOQ·February 16, 2022
PENTAX
FDA Adverse Event
Malfunction
·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code EOQ·October 22, 2021
PENTAX
FDA Adverse Event
Malfunction
·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FGB·November 30, 2021
PENTAX
FDA Adverse Event
Malfunction
·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code EOQ·July 31, 2021
COLLECT.NO.QAS KNEE IMPL.MISC./UNKNOWN
FDA Adverse Event
Injury
·AESCULAP AG·Product code JWH·January 22, 2021
PENTAX
FDA Adverse Event
Malfunction
·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code EOQ·April 22, 2022
PENTAX
FDA Adverse Event
Malfunction
·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code EOQ·July 16, 2021
PENTAX
FDA Adverse Event
Malfunction
·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code EOQ·August 5, 2021
PENTAX
FDA Adverse Event
Malfunction
·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code EOQ·July 4, 2022
PENTAX
FDA Adverse Event
Malfunction
·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code EOQ·December 14, 2022
PENTAX
FDA Adverse Event
Malfunction
·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FAJ·August 26, 2022