2,219 results · 28ms · Sources: EU EUDAMED, 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