2,219 results
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28ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Chamber Filling Capillaries
FDA UDI
BIOANALYTIC GmbH, biomed. Analysentechnik·04061609000460·
OR1 FLEXRACK, PS16B, NEO IP
FDA Adverse Event
Malfunction
·KARL STORZ SE & CO. KG·Product code LMD·November 12, 2025
LARGE BONE, HALL BLADE, OSCILLATING
FDA Adverse Event
Malfunction
·CONMED LINVATEC·Product code KFK·April 5, 2010
HALL STERUM SAW (PENUMATIC)
FDA Adverse Event
Other
·LINVATEC CORP.·Product code KFK·June 1, 2005
HALL STERNUM SAW (PNEUMATIC)
FDA Adverse Event
Death
·LINVATEC CORP·Product code KFK·May 12, 1999
STERNUM SAW BLADE GUARD
FDA Adverse Event
Malfunction
·CONMED CORPORATION·Product code KFK·July 31, 2020
STERNUM SAW BLADE GUARD
FDA Adverse Event
Malfunction
·CONMED LINVATEC·Product code KFK·January 11, 2007
OP80 SAGITTAL SAW
FDA Adverse Event
Injury
·STRYKER INSTRUMENTS·Product code KFK·May 1, 1997
MOCRO SAGITTAL SAW
FDA Adverse Event
Injury
·STRYKER INSTRUMENTS·Product code KFK·May 28, 1997
STERNUM SAW HANDPIECE
FDA Adverse Event
Malfunction
·CONMED CORPORATION·Product code KFK·July 10, 2018
BLADE TRITON 8MM GRAFT HARVEST
FDA Adverse Event
Injury
·MDT POWERED SURGICAL SOLUTIONS·Product code KFK·October 22, 2012
HALL STERUM
FDA Adverse Event
Malfunction
·CONMED CORPORATION·Product code KFK·December 18, 2012
CODMAN MODULAR AIR DRIVER
FDA Adverse Event
Malfunction
·J&J PROF, INC·Product code KFK·December 28, 2012
HALL STERNUM SAW (PNEUMATIC)
FDA Adverse Event
Malfunction
·LINVATEC CORP.·Product code KFK·August 5, 2005
HALL STERNUM SAW (PNEUMATIC)
FDA Adverse Event
Death
·LINVATEC CORPORATION·Product code KFK·August 5, 2005
STERNUM SAW HANDPIECE
FDA Adverse Event
Injury
·CONMED LARGO·Product code KFK·October 28, 2022
DRILL/REAMER
FDA Adverse Event
Malfunction
·SMITH & NEPHEW, INC.·Product code KFK·June 2, 2016
ZIMMER-HALL STERNUM SAW
FDA Adverse Event
Death
·ZIMMER HALL SURGICAL·Product code KFK·March 30, 1999
ConMed Linvatec Sternum Saw Collet Nut, Catalog Number 5059-09: Used on ConMed Linvatec Sternum Saw Handpieces (ConMed Linvatec, Hall. Versipower, Versipower Plus Handpieces) and sold individually.
FDA Recall
Terminated
·Linvatec Corp.·Product code KFK·December 20, 2005
Saw, Pneumatically Powered
FDA classification
FDA Class 1
·Saw, Pneumatically Powered