105 results
·
76ms
·
Sources: EU EUDAMED, US FDA
SAFETY-MED PRODUCTS, INC.
FDA registration
SAFETY-MED PRODUCTS, INC.·4 products·🇺🇸 United States
DIALOG+
FDA Adverse Event
Death
·B. BRAUN AVITUM AG - MELSUNGEN·Product code KDI·August 26, 2020
UNK_SMART TOUCH BIDIRECTIONAL SF
FDA Adverse Event
Injury
·BIOSENSE WEBSTER INC·Product code LPB·March 1, 2023
UNK_SMART TOUCH BIDIRECTIONAL SF
FDA Adverse Event
Injury
·BIOSENSE WEBSTER INC·Product code LPB·March 20, 2024
INTROCAN SAFETY
FDA Adverse Event
Malfunction
·B. BRAUN MELSUNGEN AG·Product code FOZ·August 26, 2014
COIL-THERMO MECHANICAL
FDA Adverse Event
Injury
·MEDOS INTERNATIONAL SARL·Product code KRD·September 3, 2019
THERMOCOOL SMARTTOUCH SF
FDA Adverse Event
Injury
·BIOSENSE WEBSTER INC·Product code LPB·August 28, 2024
QDOT MICRO
FDA Adverse Event
Injury
·BIOSENSE WEBSTER INC·Product code OAE·August 28, 2024
MONOJECT SAFETY NDL 25 X 1
FDA Adverse Event
Malfunction
·CARDINAL HEALTH·Product code FMI·October 26, 2023
LASSO¿ ELECTROPHYSIOLOGY CATHETER
FDA Adverse Event
Injury
·BIOSENSE WEBSTER INC·Product code DRF·October 12, 2022
UNK_SMART TOUCH BIDIRECTIONAL SF
FDA Adverse Event
Injury
·BIOSENSE WEBSTER INC·Product code LPB·February 13, 2023
THERMOCOOL® SMART TOUCH¿ ELECTROPHYSIOLOGY CATHETER
FDA Adverse Event
Injury
·BIOSENSE WEBSTER INC·Product code LPB·October 12, 2022
ELAN 4 1-RING DIAMOND BURR X-COARSE D6.0
FDA Adverse Event
Malfunction
·AESCULAP AG·Product code GEY·March 1, 2017
ELAN 4 1-RING DIAMOND BURR X-COARSE D5.0
FDA Adverse Event
Malfunction
·AESCULAP AG·Product code GEY·March 1, 2017
ELAN 4 1-RING DIAMOND BURR D6.0
FDA Adverse Event
Malfunction
·AESCULAP AG·Product code GEY·March 1, 2017
ON-Q PAIN RELIEF SYSTEM WITH SELECT-A-FLOW, 400 ML, 2-14 ML/HR
FDA Adverse Event
Malfunction
·AVANOS MEDICAL, INC.·Product code MEB·December 12, 2020
NOVA MIGHTY MACK ROLLATOR
FDA Adverse Event
Malfunction
·NOVA ORTHO-MED INC.·Product code ITJ·April 26, 2013
BD SAFETYGLIDE
FDA Adverse Event
Malfunction
·BECTON DICKINSON·Product code FMI·March 3, 2025
PROLENE POLYPROPYLENE SUTURE UNKNOWN PRODUCT
FDA Adverse Event
Injury
·ETHICON INC.·Product code GAW·March 6, 2024
NI
FDA Adverse Event
Malfunction
·RUBBERMAID COMMERICAL PRODUCTS, INC.·Product code IPS·February 18, 1998