25 results · 24ms · Sources: EU EUDAMED, 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