25 results
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24ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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DENTAL OPERATIVE UNIT ACCESORIES
FDA 510(k)
FDA Class 1
·Dental
OXLIFE
FDA 510(k)
FDA Class 2
·Anesthesiology
MODEL 479-01 PACING LEAD
FDA 510(k)
FDA Class 3
·Cardiovascular
COATED VICRYL (POLYGLACTIN 910)SUTURE
FDA Adverse Event
Injury
·ETHICON, INC.·Product code GAM·April 25, 2006
COATED VICRYL (POLYGLACTIN 910) SUTURE
FDA Adverse Event
Injury
·ETHICON, INC.·Product code GAM·April 25, 2006
COATED VICRYL (POLYGLACTIN 910) SUTURE
FDA Adverse Event
Injury
·ETHICON, INC.·Product code GAM·April 25, 2006
COATED VICRYL (POLYGLACTIN 910) SUTURE
FDA Adverse Event
Injury
·ETHICON, INC.·Product code GAM·April 25, 2006
COATED VICRYL (POLYGLACTIN 910) SUTURE
FDA Adverse Event
Injury
·ETHICON, INC.·Product code GAM·May 3, 2006
COATED VICRYL ( POLYGLACTIN 910) SUTURE
FDA Adverse Event
Injury
·ETHICON, INC.·Product code GAM·May 5, 2006
COATED VICRYL (POLYGLACTIN 910) SUTURE
FDA Adverse Event
Injury
·ETHICON, INC.·Product code GAM·May 5, 2006
COATED VICRYL (POLYGLACTIN 910) SUTURE
FDA Adverse Event
Other
·ETHICON, INC.·Product code GAM·May 26, 2006
COATED VICRYL (POLYGLACTIN 910) SUTURE
FDA Adverse Event
Injury
·ETHICON, INC.·Product code GAM·April 25, 2006
MEDFUSION 3500 SYRINGE INFUSION PUMP
FDA Adverse Event
Malfunction
·SMITHS MEDICAL·Product code FRN·May 8, 2014
PERCLOSE PROGLIDE 6F SUTURE MEDIATED CLOSURE (SMC) SYSTEM
FDA Adverse Event
Injury
·AV-TEMECULA-CT·Product code MGB·February 5, 2013
9800
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·December 6, 2010
JAWS "HIQ+", 5 X 330 MM, GRASPING FORCEPS, CROCEOLMI
FDA Adverse Event
Malfunction
·OLYMPUS WINTER & IBE GMBH·Product code HET·March 15, 2023
JAWS "HIQ+", 5 X 330 MM, SCISSORS, METZENBAUM
FDA Adverse Event
Malfunction
·OLYMPUS WINTER & IBE GMBH·Product code HET·March 30, 2023
3.0MM TI CERVICAL SPINE LOCKING SCREW 16MM
FDA Adverse Event
Malfunction
·SYNTHES, USA·Product code KWQ·November 3, 2016
2.0MM ANGLED AWL
FDA Adverse Event
Malfunction
·SYNTHES HAGENDORF·Product code KWQ·November 3, 2016
SHAFT "HIQ+", 5 X 330 MM
FDA Adverse Event
Malfunction
·OLYMPUS WINTER & IBE GMBH·Product code HET·May 23, 2023