9,964 results · 34ms · Sources: EU EUDAMED, 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