13 results · 39ms · 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.

BALL HEADS: MECTACER BIOLOX DELTA CERAMIC BALL HEAD 12/14 32 SIZE S

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code LZO·October 30, 2020

BIPOLAR MACRO FORCEPS D:5/ 310MM

FDA Adverse Event
Malfunction ·AESCULAP AG & CO KG·Product code GEI·April 6, 2015

BIPOLAR MARYLAND DISS.FCPS 5MM 310MM

FDA Adverse Event
Malfunction ·AESCULAP AG & CO KG·Product code GEI·March 9, 2015

MPACT ACETABULAR SYSTEM

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code LPH·March 10, 2026

JAW INS.BIP.MARYLAND DISS.FEN.5/310MM

FDA Adverse Event
Malfunction ·AESCULAP AG & CO. KG·Product code GEI·August 29, 2014

JAW INS. BIP.MARYLAND DISS.FEN.5/310MM

FDA Adverse Event
Malfunction ·AESCULAP AG & CO. KG.·Product code GEI·January 13, 2015

WAVEWRITER ALPHA?

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC NEUROMODULATION CORPORATION·Product code LGW·December 6, 2024

MARYLAND GSP.FORCEPS FEN.5/310MM HF CON.

FDA Adverse Event
Malfunction ·AESCULAP AG & CO. KG·Product code GEI·February 19, 2014

JAW INS.BIP.MARYLAND DISS.FEN.5/310MM

FDA Adverse Event
Malfunction ·AESCULAP AG & CO. KG·Product code GEI·August 13, 2015

ENDO STITCH POLYSORB 0 48 VIO DLU SU

FDA Adverse Event
Injury ·COVIDIEN, FORMERLY US SUR·Product code KOG·March 6, 2013

OPTIFLUX 200NRE DIALYZER FINISHED ASSY.

FDA Adverse Event
Malfunction ·FRESENIUS MEDICAL CARE NORTH AMERICA·Product code FJI·July 21, 2014

*

FDA Adverse Event
Malfunction ·OR SOLUTIONS, INC.·Product code KKX·January 24, 2008

MARYLAND GSP.FORCEPS FEN.5/310MM HF.CON.

FDA Adverse Event
Malfunction ·AESCULAP, INC.·Product code GEI·August 21, 2015