89 results
·
28ms
·
Sources: EU EUDAMED, US FDA
Reprocessed Advisor HD Grid Mapping Catheter, Sensor Enabled
FDA 510(k)
FDA Class 2
·Cardiovascular
D-10
FDA UDI
BIO-RAD LABORATORIES, INC.·00847817003462·D-10 Analytical Cartridge Hemoglobin A1c Progra...
MIS Beveled Screw
FDA UDI
Treace Medical Concepts, Inc.·00810111222822·MIS Screw 3mm Driver
OPERATING SCISSORS
FDA UDI
SONTEC INSTRUMENTS, INC.·00192896054547·OPERATING SCISSORS STRAIGHT BLUNT TIPS POWER CU...
10PW - General Purpose
FDA UDI
Certified Safety Manufacturing, Inc.·00766588020129·10PW - General Purpose
KSEA CHARDONNES MORCELLATION KNIFE
FDA 510(k)
FDA Class 1
·Obstetrics/Gynecology
DENTACENTER/EXPEDITION, MODEL SAF-430
FDA 510(k)
FDA Class 1
·Dental
TOWEL OR 17X24IN BLUE STERILE 4/PK
FDA Adverse Event
Malfunction
·CARDINAL HEALTH SHANGHAI·Product code FRL·July 7, 2020
PRECISION TUNA OFFICE
FDA Adverse Event
Other
·VIDAMED, INC.·Product code KNS·March 29, 2002
T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY
FDA Adverse Event
Malfunction
·TANDEM DIABETES CARE·Product code QFG·July 6, 2023
T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY
FDA Adverse Event
Malfunction
·TANDEM DIABETES CARE·Product code QFG·February 1, 2022
T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY
FDA Adverse Event
Malfunction
·TANDEM DIABETES CARE·Product code QFG·December 15, 2021
T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY
FDA Adverse Event
Malfunction
·TANDEM DIABETES CARE·Product code QFG·August 18, 2022
ENDOPATH DILATING TIP TROCAR
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, INC.·Product code GCJ·May 8, 1998
T:SLIM X2 INSULIN PUMP WITH BASAL-IQ TECHNOLOGY
FDA Adverse Event
Malfunction
·TANDEM DIABETES CARE·Product code OZO·August 13, 2019
SYNCHROMED EL
FDA Adverse Event
Death
·MEDTRONIC INC.·Product code LKK·August 8, 2002
HARMONIC SCALPEL LAPAROSONIC COAGULATING SHEARS
FDA Adverse Event
Injury
·EES-SMITHFIELD·Product code KNS·March 12, 1998
T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY
FDA Adverse Event
Malfunction
·TANDEM DIABETES CARE·Product code QFG·October 25, 2023
DISPOSABLE FAST CONTROL COAGULATION SUCTION TUBE
FDA Adverse Event
Injury
·WECK CLOSURE SYSTEMS·Product code GEI·February 2, 2001
BD VACUTAINER® PUSH BUTTON BLOOD COLLECTION SET
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO., (BD)·Product code JKA·December 8, 2023