34 results
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27ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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HeatLux Pro II
FDA 510(k)
FDA Class 2
·Physical Medicine
KMEDIC
FDA UDI
TELEFLEX INCORPORATED·24026704283549·LAHEY FINGER RETRACTOR 4 3/4" 3 PRONG SHARP
BREATHING FILTER BACTERIAL/VIRAL, MODEL AG7178
FDA 510(k)
FDA Class 2
·Anesthesiology
TYVEK SELF-SEAL POUCHES ,TYVEK HEAT-SEAL ROLLS
FDA 510(k)
FDA Class 2
·General Hospital
PELVICOL ACEELUAR COLLAGEN MATRIX
FDA Adverse Event
Injury
·TISSUE SCIENCE LABORATORIES·Product code FTL·May 29, 2013
COLLEAGUE PRE 1.7
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·July 7, 2011
TRANSDUCER LINE SET-TRIPLE SET
FDA Adverse Event
Other
·EDWARDS LIFESCIENCES CORP.·Product code DRS·September 4, 2008
SHIDEN HP
FDA Adverse Event
Injury
·KANEKA CORPORATION·Product code LIT·June 4, 2019
OHICHO3
FDA Adverse Event
Injury
·KANEKA CORPORATION·Product code LIT·August 30, 2022
KYPHON BONE CEMENT
FDA Adverse Event
Injury
·MEDTRONIC SOFAMOR DANEK USA, INC.·Product code NDN·April 23, 2019
OHICHO3
FDA Adverse Event
Injury
·KANEKA CORPORATION·Product code LIT·March 18, 2026
METACROSS OTW PTA BALLOON DILATATION CATHETER
FDA Adverse Event
Injury
·KANEKA CORPORATION·Product code LIT·August 19, 2019
1030489-2019-01423
FDA Adverse Event
Injury
·MEDTRONIC SOFAMOR DANEK·Product code NDN·December 13, 2019
SHIDEN HP
FDA Adverse Event
Injury
·KANEKA CORPORATION·Product code LIT·March 1, 2024
OHICHO NEO
FDA Adverse Event
Injury
·KANEKA CORPORATION·Product code LIT·February 7, 2024
SHIDEN
FDA Adverse Event
Injury
·KANEKA CORPORATION·Product code LIT·July 10, 2020
OHICHO3
FDA Adverse Event
Injury
·Product code LIT·December 26, 2019
DIVA
FDA Adverse Event
Injury
·KANEKA CORPORATION·Product code LIT·July 7, 2020
DIVA
FDA Adverse Event
Injury
·KANEKA CORPORATION·Product code LIT·July 7, 2020
SHIRANUI EX
FDA Adverse Event
Injury
·KANEKA CORPORATION·Product code LIT·August 12, 2020