22 results · 18ms · Sources: EU EUDAMED, US FDA

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MODIFICATION TO ACCESS CEA REAGENTS FOR USE ON THE ACCESS IMMUNOASSAY ANALYZER, MODELS 33200, 33205, 33209, 33206

FDA 510(k)
FDA Class 2 ·Immunology

FORTRESS COMMUTER FT (FOLDING TRANSPORT)

FDA 510(k)
FDA Class 2 ·Physical Medicine

CENTRIA INSULIN RIA

FDA 510(k)
FDA Class 1 ·Clinical Chemistry

MICROTAINER SST GOLD

FDA Adverse Event
Malfunction ·BD CARIBE LTD.·Product code JKA·June 7, 2018

BD MICROTAINER® EDTA LAVENDAR TUBES

FDA Adverse Event
Malfunction ·BD CARIBE LTD.·Product code JKA·May 1, 2018

BD MICROTAINER® EDTA LAVENDAR TUBES

FDA Adverse Event
Malfunction ·BD CARIBE LTD.·Product code JKA·May 16, 2018

MICROTAINER SST GOLD

FDA Adverse Event
Malfunction ·BECTON DICKINSON CARIBE LTD·Product code JKA·May 7, 2018

BD MICROTAINER® EDTA LAVENDER TUBES

FDA Adverse Event
Malfunction ·BD CARIBE LTD.·Product code JKA·April 27, 2018

BD MICROTAINER® EDTA LAVENDAR TUBES

FDA Adverse Event
Malfunction ·BD CARIBE LTD.·Product code JKA·May 3, 2018

BD MICROTAINER® BLOOD COLLECTION TUBES

FDA Adverse Event
Malfunction ·BD CARIBE LTD.·Product code JKA·December 3, 2017

PROFEMUR(R) TL STEM

FDA Adverse Event
Injury ·WRIGHT MEDICAL TECHNOLOGY, INC.·Product code KWA·March 6, 2013

CONCERTO CRT-D DR

FDA Adverse Event
Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code NIK·August 8, 2014

ADAPTA DR

FDA Adverse Event
Malfunction ·MEDTRONIC MED REL, INC.·Product code NVZ·February 15, 2011

UNKNOWN SPIRALOK ANCHOR

FDA Adverse Event
Injury ·DEPUY MITEK·Product code MBI·June 21, 2007

PENTAX

FDA Adverse Event
Injury ·PENTAX·Product code EOQ·January 10, 2017

PENTAX

FDA Adverse Event
Injury ·PENTAX·Product code EOQ·January 10, 2017

PENTAX

FDA Adverse Event
Injury ·PENTAX·Product code EOQ·January 10, 2017

PENTAX

FDA Adverse Event
Injury ·PENTAX·Product code EOQ·January 10, 2017

PENTAX

FDA Adverse Event
Injury ·PENTAX·Product code EOQ·January 10, 2017

PENTAX

FDA Adverse Event
Injury ·PENTAX·Product code EOQ·January 10, 2017