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BYG INFORMATIQUE

FDA registration
BYG INFORMATIQUE·1 product·🇫🇷 France

Ypoc

FDA UDI
BYG INFORMATIQUE·03770035155019·Middleware dedicated to EBMD management. The pr...

Lab Composer

FDA UDI
BYG INFORMATIQUE·03770035155057·Lab Composer is a software middleware intended ...

nYna

FDA UDI
BYG INFORMATIQUE·03770035155002·nYna is a unique solution, both technologically...

POC Controller

FDA UDI
BYG INFORMATIQUE·03770035155064·POC Controller is a software middleware intende...

ALINITY C-I SERIES SYSTEM

FDA Adverse Event
Malfunction ·ABBOTT GERMANY·Product code JJE·July 30, 2018

PHOTOFIX DECELLULARIZED BOVINE PERICARDIUM - UNKNOWN CONFIGURATION

FDA Adverse Event
Injury ·ARTIVION, INC.·Product code DXZ·November 19, 2024

CCASC LAPAROTOMY PACK

FDA Adverse Event
Malfunction ·DEROYAL INDUSTRIES, INC..·Product code LRO·August 7, 2024

KANGAROO EPUMP - RFB

FDA Adverse Event
Injury ·COVIDIEN·Product code LZH·February 13, 2017

SYNCHROMED II

FDA Adverse Event
Injury ·MDT PUERTO RICO OPERATIONS CO·Product code LKK·June 16, 2017

UNKNOWN IVS TUNNELLER DEVICE

FDA Adverse Event
Injury ·BALLYMONEY - USS·Product code FTL·July 24, 2014

UNKNOWN IVS TUNNELLER DEVICE

FDA Adverse Event
Injury ·BALLYMONEY - USS·Product code FTL·July 24, 2014

KYPHX HV-R BONE CEMENT

FDA Adverse Event
Malfunction ·MEDTRONIC SPINE LLC·Product code NDN·September 14, 2010

KYPHX? HV-R? BONE CEMENT

FDA Adverse Event
Malfunction ·MEDTRONIC SPINE LLC·Product code NDN·November 12, 2010

KYPHX INFLATABLE BONE TAMP

FDA Adverse Event
Injury ·MEDTRONIC SPINE LLC.·Product code HXG·October 13, 2009

COBAS INTEGRA 800

FDA Adverse Event
Malfunction ·ROCHE DIAGNOSTICS·Product code JJE·August 8, 2013

KYPHON INFLATABLE BONE TAMP

FDA Adverse Event
Injury ·MEDTRONIC SOFAMOR DANEK·Product code HRX·April 3, 2012

KYPHX HV-R BONE CEMENT

FDA Adverse Event
Injury ·MEDTRONIC SPINE LLC.·Product code NDN·December 2, 2009

UNKNOWN HIP FEMORAL HEAD

FDA Adverse Event
Injury ·DEPUY ORTHOPAEDICS, INC. 1818910·Product code JDI·May 31, 2019

UNKNOWN HIP ACETABULAR LINERS

FDA Adverse Event
Injury ·DEPUY ORTHOPAEDICS, INC. 1818910·Product code KWA·May 31, 2019