12 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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HANDHELD ECG MONITOR, MODEL MD100
FDA 510(k)
FDA Class 2
·Cardiovascular
Cervical
FDA UDI
MEDTRONIC SOFAMOR DANEK, INC.·00613994255198·CASE 7080933 INSTR OUTER LID
SchureMed
FDA UDI
SCHUERCH CORPORATION·00810014608389·ALLEN, STERIS-AMSCO 4.25"DELUXE GEL
FAST-FIX 360 CURVED NDL DELIVERY SYS
FDA Adverse Event
Injury
·SMITH & NEPHEW, INC.·Product code GAT·August 18, 2022
FAST-FIX 360 CURVED NDL DELIVERY SYS
FDA Adverse Event
Injury
·SMITH & NEPHEW, INC.·Product code GAT·August 18, 2022
SEAL-ON TOPICAL HEMPSTATIC POWDER SPRAY
FDA 510(k)
FDA Unclassified
·Unknown
GARAVENTA SUPER-TRAC TRE-52
FDA 510(k)
FDA Class 2
·Physical Medicine
REBOUND HRD
FDA Adverse Event
Malfunction
·MINNESOTA MEDICAL DEVELOPMENT, INC.·Product code FTL·May 16, 2011
UNIVERSAL MODULAR ELECTRIC/BATTERY SINGLE
FDA Adverse Event
Malfunction
·ZIMMER SURGICAL S.A.·Product code HAB·April 24, 2013
CARPENTIER-MCCARTHY-ADAMS IMR ETLOGIX MITRAL ANNULOPLASTY RING
FDA Adverse Event
Injury
·EDWARDS LIFESCIENCES·Product code KRH·May 8, 2011
PINN MAR +4 NEUT 32IDX56OD
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS, INC.·Product code LPH·July 22, 2008
FAST-FIX 360 CURVED NDL DELIVERY SYS
FDA Adverse Event
Injury
·SMITH & NEPHEW, INC.·Product code GAT·August 18, 2022