111 results · 65ms · Sources: EU EUDAMED, US FDA

Get notified when this changes

We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

BRASSLER USA MEDICAL, LLC MILLING HANDPIECE

FDA Adverse Event
Malfunction ·BRASSELER USA, MEDICAL L.L.C.·Product code HSZ·August 11, 2015

BRASSELER USA MEDICAL, LLC MILING HANDPIECE

FDA Adverse Event
Malfunction ·BRASSELER USA, MEDICAL L.L.C.·Product code HSZ·November 21, 2014

BRASSERLER USA MEDICAL, LLC MILLING HANDPIECE

FDA Adverse Event
Malfunction ·BRASSELER USA, MEDICAL L.L.C.·Product code HSZ·May 29, 2015

ZIMMER MILLBRASSERLER USA MEDICAL, LLC MILLING HANDPIECE

FDA Adverse Event
Malfunction ·BRASSELER USA, MEDICAL L.L.C.·Product code HSZ·January 29, 2016

ZIMMER MILLBRASSERLER USA MEDICAL, LLC MILLING HANDPIECE

FDA Adverse Event
Malfunction ·BRASSELER USA, MEDICAL L.L.C.·Product code HSZ·January 29, 2016

BRASSELER USA TWIST DRILL

FDA Adverse Event
Malfunction ·BRASSELER USA, MEDICAL, LLC·Product code HBE·May 21, 2013

BRASSELER USA TWIST DRILL

FDA Adverse Event
Malfunction ·BRASSELER USA, MEDICAL, LLC·Product code GFF·September 22, 2014

BRASSELER USA SURGICAL BUR

FDA Adverse Event
BRASSELER USA MEDICAL, LLC·Product code GFF·August 29, 2019

SERVO-I

FDA Adverse Event
Death ·MAQUET CRITICAL CARE AB·Product code CBK·October 25, 2018

POWERLED

FDA Adverse Event
Injury ·MAQUET SAS·Product code FSY·April 30, 2018

SERVO-I

FDA Adverse Event
Malfunction ·MAQUET CRITICAL CARE AB·Product code CBK·December 11, 2018

SERVO-I

FDA Adverse Event
Malfunction ·MAQUET CRITICAL CARE AB·Product code CBK·December 21, 2018

SERVO-U

FDA Adverse Event
Malfunction ·MAQUET CRITICAL CARE AB·Product code CBK·November 30, 2018

SERVO-I

FDA Adverse Event
Malfunction ·MAQUET CRITICAL CARE AB·Product code CBK·October 12, 2018

FLOW-I C20

FDA Adverse Event
Injury ·MAQUET CRITICAL CARE AB·Product code CBK·May 31, 2018

SERVO-I

FDA Adverse Event
Malfunction ·MAQUET CRITICAL CARE AB·Product code CBK·May 21, 2019

CELT ACD VASCULAR CLOSURE DEVICE

FDA Adverse Event
Injury ·VASORUM LTD·Product code MGB·June 12, 2019

ONE EARTH HEALTH KETONE TEST STRIPS

FDA Adverse Event
Malfunction ·UNK·Product code JIN·December 6, 2018

SERVO-U

FDA Adverse Event
Injury ·MAGNUS LINDQVIST·Product code CBK·August 10, 2018

LIFESTYLES SKYN

FDA Adverse Event
Injury ·SURETEX LTD.·Product code MOL·April 17, 2015