48 results · 23ms · Sources: EU EUDAMED, US FDA

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PANPAC VAGINAL PESSARY

FDA 510(k)
FDA Class 2 ·Obstetrics/Gynecology

ULTRACISION HARMONIC SCALPEL COAGULATING SHEARS, MODEL LCSC5,LCSC1,CS23C,CS231,CS14C,CS141,LCSB5,LCSK5,LCS15,LCS16,CS150

FDA 510(k)
FDA Class 2 ·General, Plastic Surgery

INION CPS 2.5/2.8 SCREW

FDA 510(k)
FDA Class 2 ·Orthopedic

ULTRACISION SURG DEV, CURVED SHEARS, OPEN

FDA Adverse Event
Malfunction ·ETHICON ENDO SURGERY, INC.(CINCINNATI)·Product code LFL·June 7, 2006

ULTRACISION SURG DEV, CURVED SHEARS, ENDO

FDA Adverse Event
Malfunction ·ETHICON ENDO SURGERY, INC.(CINCINNATI)·Product code LFL·June 7, 2006

ULTRACISION SURG DEV, CURVED SHEARS, ENDO

FDA Adverse Event
Malfunction ·ETHICON ENDO-SURGERY, INC.(CINCINNATI)·Product code LFL·June 2, 2006

ULTRACISION SURG DEV, CURVED SHEARS, OPEN

FDA Adverse Event
Malfunction ·ETHICON ENDO SURGERY, INC.(CINCINNATI)·Product code GEI·June 19, 2006

ULTRACISION SURG DEV, CURVED SHEARS, ENDO

FDA Adverse Event
Malfunction ·ETHICON ENDO SURGERY, INC.(CINCINNATI)·Product code LFL·June 19, 2006

ULTRACISION SURG DEV, CURVED SHEARS, ENDO

FDA Adverse Event
Malfunction ·ETHICON ENDO SURGERY, INC.(CINCINNATI)·Product code LFL·June 19, 2006

ULTRACISION SURG DEV, CURVED SHEARS, ENDO

FDA Adverse Event
Malfunction ·ETHICON ENDO SURGERY, INC.(CINCINNATI)·Product code GEI·June 19, 2006

ULTRACISION SURG DEV, CURVED SHEARS, OPEN

FDA Adverse Event
Malfunction ·ETHICON ENDO SURGERY, INC.(CINCINNATI)·Product code LFL·June 7, 2006

SYNCHROMED II

FDA Adverse Event
Injury ·MDT PUERTO RICO OPERATIONS CO·Product code LKK·May 3, 2013

ONETOUCHPING GLUCOSEMGMTSYSTEM

FDA Adverse Event
Malfunction ·ANIMAS CORPORATION·Product code LZG·September 16, 2014

GREENLIGHT ADDSTAT

FDA Adverse Event
Malfunction ·AMERICAN MEDICAL SYSTEMS, INNOVATION CENTER - SILICON VALLEY·Product code GEX·May 5, 2011

ULTRACISION SURG DEV, CURVED SHEARS, ENDO

FDA Adverse Event
Malfunction ·ETHICON ENDO SURGERY, INC.(CINCINNATI)·Product code GEI·June 19, 2006

INRATIO2 PT MONITORING SYSTEM

FDA Adverse Event
Malfunction ·ALERE SAN DIEGO, INC.·Product code GJS·September 11, 2015

INRATIO2 PT MONITORING SYSTEM

FDA Adverse Event
Injury ·ALERE SAN DIEGO, INC.·Product code GJS·September 14, 2015

INRATIO2 PT MONITORING SYSTEM

FDA Adverse Event
Malfunction ·ALERE SAN DIEGO, INC.·Product code GJS·August 3, 2015

INRATIO2 PT MONITORING SYSTEM

FDA Adverse Event
Malfunction ·ALERE SAN DIEGO, INC.·Product code GJS·February 4, 2015

INRATIO2 PT MONITORING SYSTEM

FDA Adverse Event
Malfunction ·ALERE SAN DIEGO, INC.·Product code GJS·October 8, 2015