9 results
·
34ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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CD Horizon ModuLeX FNS Screw Set (Fenestrated Screw); CD Horizon ModuLeX Spinal System (Modular Extended Tab Head)
FDA 510(k)
FDA Class 2
·Orthopedic
ONE OTUCH ULTRA
FDA Adverse Event
Malfunction
·LIFESCAN, INC.·Product code CFR·July 3, 2002
ONE TOUCH BASIC
FDA Adverse Event
Malfunction
·LIFESCAN, INC.·Product code CFR·July 16, 2003
SECUMAX BLOOD COLLECTION SYSTEM
FDA 510(k)
FDA Class 2
·General Hospital
BEAUTIFIL BULK FLOWABLE
FDA 510(k)
FDA Class 2
·Dental
UNSPECIFIED SAFESET TRANSPAC SETS
FDA Adverse Event
Malfunction
·ICU MEDICAL DE MEXICO, S. DE R.L. DE C.V.·Product code DRS·January 2, 2025
CENTURY BED
FDA Adverse Event
Malfunction
·HILL-ROM RITTER·Product code FNL·November 4, 2008
COLLEAGUE
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·September 2, 2011
SELOX SR 53
FDA Adverse Event
Injury
·BIOTRONIK SE & CO. KG·Product code NVN·July 17, 2013