35 results
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26ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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ENA HFO COMPOSITE SYSTEM
FDA 510(k)
FDA Class 2
·Dental
ORTHOPEDIC MANUAL SURGICAL INSTRUMENT
FDA UDI
FX SOLUTIONS·03701037313510·STABILITY TRIAL CUP FOR BOACH Ø32+6
STANDARD TR...
ANIMEC, MODELS AM-2S-4 AND AM-2S-5
FDA 510(k)
FDA Class 2
·General Hospital
ULTRACISION HARMONIC SCALPEL SYSTEM, MODELS GEN01, GEN02, GEN03, HP052, HP053, HSA07
FDA 510(k)
FDA Unclassified
·Unknown
ULTRACISION HARMONIC SCALPEL HAND PIECE
FDA Adverse Event
Malfunction
·ETHICON ENDO SURGERY, INC.(CINCINNATI)·Product code LFL·June 13, 2006
ULTRACISION SURGERY REUSABLE DEVICES, HANDPIECE 54, 55
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, INC. (CINCINNATI)·Product code LFL·June 15, 2006
ULTRACISION SURGERY REUSABLE DEVICES, HANDPIECE 54,55
FDA Adverse Event
Malfunction
·ETHICON ENDO SURGERY, INC.(CINCINNATI)·Product code LFL·June 19, 2006
ULTRACISION SURGERY REUSABLE DEVICES, HANDPIECE 54,55
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, INC.(CINCINNATI)·Product code LFL·June 15, 2006
ULTRACISION SURGERY REUSABLE DEVICES, HANDPIECE 54, 55
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, INC.(CINCINNATI)·Product code LFL·June 15, 2006
ULTRACISION HARMONIC SCALPEL HAND PIECE
FDA Adverse Event
Malfunction
·ETHICON ENDO SURGERY, INC.(CINCINNATI)·Product code LFL·June 7, 2006
ULTRACISION SURGERY REUSABLE DEVICES, HANDPIECE 54,55
FDA Adverse Event
Malfunction
·ETHICON ENDO SURGERY, INC.(CINCINNATI)·Product code LFL·June 7, 2006
ULTRACISION SURGERY REUSABLE DEVICES, HANDPIECE 54, 55
FDA Adverse Event
Malfunction
·ETHICON ENDO SURGERY, INC. (CINCINNATI)·Product code LFL·June 7, 2006
ULTRACISION SURGERY REUSABLE DEVICES, HANDPIECE 54,55
FDA Adverse Event
Malfunction
·ETHICON ENDO SURGERY, INC.(CINCINNATI)·Product code LFL·June 19, 2006
ULTRACISION SURGERY REUSABLE DEVICES, HANDPIECE 54,55
FDA Adverse Event
Malfunction
·ETHICON ENDO SURGERY, INC.(CINCINNATI)·Product code LFL·June 7, 2006
ULTRACISION HARMONIC SCALPEL HAND PIECE
FDA Adverse Event
Malfunction
·ETHICON ENDO SURGERY, INC.(CINCINNATI)·Product code LFL·June 13, 2006
BD PHOENIX¿ SMIC-101
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·February 13, 2026
ULTRACISION SURGERY REUSABLE DEVICES, HANDPIECE 54,55
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, INC.(CINCINNATI)·Product code LFL·June 16, 2006
PARADYM
FDA Adverse Event
Injury
·SORIN C.R.M., S.R.L.·Product code MRM·April 12, 2013
7900
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS GMBH·Product code JAA·March 21, 2011
PRECISION
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC NEUROMODULATION CORP·Product code LGW·June 19, 2008