80 results
·
87ms
·
Sources: EU EUDAMED, US FDA
Oral and nose care
Basic UDI-DI
EU MDR
·
Eu Md Class 1
·Inter.med·41 devices
ORALBPWRRCHGTOOTHBRUSHHANDLE3767SMART5000
FDA Adverse Event
Malfunction
·BRAUN GMBH WERK MARKTHEIDENFELD·Product code JEQ·March 3, 2023
ORALBPWRORALCARERFLSDUALACTNEB417BRUSHSET
FDA Adverse Event
Malfunction
·BRAUN GMBH WERK MARKTHEIDENFELD·Product code JEQ·June 14, 2024
ORAL-B PROFESSIONAL CARE RECHARGEABLE TOOTHBRUSH
FDA Adverse Event
Malfunction
·BRAUN GMBH WERK MARKTHEIDENFELD·Product code JEQ·September 25, 2015
RADIESSE DERMAL FILLER
FDA Adverse Event
Injury
·MERZ NORTH AMERICA·Product code LMH·August 7, 2015
ORALBPWRRCHGTOOTHBRUSHHANDLEPROCROSSACTN
FDA Adverse Event
Malfunction
·BRAUN GMBH WERK MARKTHEIDENFELD·Product code JEQ·January 9, 2017
E-TAD
FDA Adverse Event
Other
·HOLLISTER INCORPORATED·Product code CBH·October 23, 2003
BIOTENE DRY MOUTH ORAL RINSE (2013 FORMULATION
FDA Adverse Event
Death
·GLAXOSMITHKLINE·Product code LFD·November 29, 2013
RESTYLANE INJECTABLE GEL
FDA Adverse Event
Q-MED AB·Product code LMH·March 1, 2005
CAREFUSION
FDA Adverse Event
Injury
·CAREFUSION·Product code CBK·March 8, 2013
THERASPHERE®
FDA Adverse Event
Death
·BIOCOMPATIBLES UK LTD.·Product code NAW·June 16, 2017
ELECTRIC SCALPEL
FDA Adverse Event
Injury
·VONCARE MEDICAL DEVICE CO. LTD.·Product code GEI·August 28, 2025
INTL QCARE RX Q4 SYS W/CORINZ 20
FDA Adverse Event
Injury
·SAGE PRODUCTS LLC·Product code KXF·June 18, 2025
HEARTWARE VENTRICULAR ASSIST SYSTEM - PUMP
FDA Adverse Event
Injury
·HEARTWARE, INC.·Product code DSQ·May 9, 2022
SYNCHROMED EL
FDA Adverse Event
Injury
·RICE CREEK MANUFACTURING·Product code LKK·August 17, 2010
JUVEDERM ULTRA PLUS XC TSK US
FDA Adverse Event
Injury
·PRINGY·Product code LMH·February 5, 2025
ZONAS POROUS TAPES
FDA Adverse Event
Injury
·JOHNSON & JOHNSON MEDICAL (SHERMAN)·Product code KGX·March 28, 2003
UNK DERMAL FILLER
FDA Adverse Event
Injury
·PRINGY·Product code LMH·February 5, 2025
JUVEDERM VOLUMA XC 27G 2 X 1ML
FDA Adverse Event
Injury
·PRINGY·Product code LMH·February 5, 2025
SERVO-I
FDA Adverse Event
Malfunction
·MAQUET CRITICAL CARE AB·Product code CBK·October 2, 2018