9,964 results
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34ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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X-PEDION
FDA Adverse Event
Injury
·COVIDIEN (IRVINE)·Product code DQX·March 31, 2017
ONYX
FDA Adverse Event
Injury
·COVIDIEN (IRVINE)·Product code MFE·March 31, 2017
MICROCATHETER
FDA Adverse Event
Injury
·COVIDIEN (IRVINE)·Product code KRA·March 31, 2017
MICROCATHETER
FDA Adverse Event
Injury
·COVIDIEN (IRVINE)·Product code KRA·March 31, 2017
ONYX
FDA Adverse Event
Injury
·COVIDIEN (IRVINE)·Product code MFE·March 31, 2017
ONYX
FDA Adverse Event
Injury
·COVIDIEN (IRVINE)·Product code MFE·March 31, 2017
MICROCATHETER
FDA Adverse Event
Injury
·COVIDIEN (IRVINE)·Product code KRA·March 31, 2017
ONYX
FDA Adverse Event
Injury
·COVIDIEN (IRVINE)·Product code MFE·March 31, 2017
ENDURANT
FDA Adverse Event
Death
·MEDTRONIC CARDIOVASCULAR·Product code MIH·February 20, 2014
ENDURANT
FDA Adverse Event
Death
·MEDTRONIC CARDIOVASCULAR·Product code MIH·June 10, 2014
ONYX
FDA Adverse Event
Injury
·COVIDIEN (IRVINE)·Product code MFE·March 31, 2017
BD ULTRA-FINE¿ INSULIN SYRINGE
FDA Adverse Event
Malfunction
·BD MEDICAL - DIABETES CARE·Product code FMF·April 11, 2018
Novoste, Beta-Cath 3.5F System, New B-Rail 3.5F Delivery Catheter, with Indicator of Source Train (IST), Novoste Corporate, 3890 Steve Reynolds Blvd, Norcross, GA 30093, Tel: +1770-717-0904, Fax: +1770-717-1283, 1-800-NOVOSTE (1-800-668-6783), www.novoste.com.
FDA Recall
Terminated
·Novoste Corporation·Product code JAJ·January 25, 2002
JAC CUSTOM POUCHES
FDA registration
JAC CUSTOM POUCHES·4 products·🇺🇸 United States
JAI SURGICALS LTD.
FDA registration
JAI SURGICALS LTD.·7 products·🇮🇳 India
JAC-CELL MEDIC
FDA registration
JAC-CELL MEDIC·1 product·🇨🇦 Canada
JAI
FDA 510(k)
FDA Class 1
·General Hospital
BAC JAC
FDA 510(k)
FDA Class 1
·Orthopedic
JAK DIVERSIFIED II, INC.
FDA registration
JAK DIVERSIFIED II, INC.·3 products·🇺🇸 United States
Gold Lion Water-Base 8oz
FDA UDI
JAD PARTNERS CORP.·00860015384416·Water-Based Personal Lubricant