42 results
·
22ms
·
Sources: EU EUDAMED, US FDA
Emprint SX Ablation Platform with Thermosphere Technology
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
LOJIC+
FDA UDI
SDI LIMITED·09336472001704·LOJIC+ 3SP REG 50
LOJIC+
FDA UDI
SDI LIMITED·DO3642033032·
Ophthalmic Cannula
FDA UDI
KATENA PRODUCTS, INC.·00841668114155·KRATZ POLISHER 23GA END (PK/10)
Ophthalmic Cannula
FDA UDI
KATENA PRODUCTS, INC.·00841668113783·AIR INJECT CANNULA 25GA
ENDOMAT LC PUMP, MODEL 20 3303 20
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
IM-5B MICROINJECTOR
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
EXPORT ASPIRATION CATHETER
FDA 510(k)
FDA Class 2
·Cardiovascular
CONMED HAND CONTROLLED BOVIE
FDA Adverse Event
CONMED·Product code GEI·November 29, 2012
GYNECARE MORCELLEX TISSUE MORCELLATOR
FDA Adverse Event
Malfunction
·ETHICON, INC.·Product code HET·October 14, 2008
MAXIMO VR
FDA Adverse Event
Injury
·MEDTRONIC MED REL, INC.·Product code LWS·August 11, 2011
LYNX SYSTEM
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC - MARLBOROUGH·Product code FTL·July 2, 2013
CHECK-IT
FDA Adverse Event
Malfunction
·PFIZER, INC.·Product code QJR·May 23, 2023
CHECK-IT
FDA Adverse Event
Malfunction
·LUCIRA HEALTH, INC.·Product code QJR·September 1, 2022
CHECK-IT
FDA Adverse Event
Malfunction
·LUCIRA HEALTH, INC.·Product code QJR·September 1, 2022
CHECK-IT
FDA Adverse Event
Malfunction
·LUCIRA HEALTH, INC.·Product code QJR·August 25, 2022
CHECK-IT
FDA Adverse Event
Malfunction
·LUCIRA HEALTH, INC.·Product code QJR·September 8, 2022
CHECK-IT
FDA Adverse Event
Malfunction
·LUCIRA HEALTH, INC.·Product code QJR·September 8, 2022
CHECK-IT
FDA Adverse Event
Malfunction
·LUCIRA HEALTH, INC.·Product code QJR·September 8, 2022
CHECK-IT
FDA Adverse Event
Malfunction
·LUCIRA HEALTH, INC.·Product code QJR·September 9, 2022