33 results · 24ms · Sources: EU EUDAMED, US FDA

Get notified when this changes

We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

CP-SLEEVE

FDA 510(k)
FDA Class 2 ·Radiology

UNBRANDED

FDA UDI
FGX INTERNATIONAL INC.·00193033545799·

BAUMER CEMENTED HIP PROSTHESIS

FDA 510(k)
FDA Class 2 ·Orthopedic

ECLIPSE 6.5

FDA 510(k)
FDA Class 2 ·Radiology

BD VACUTAINER® PLUS CITRATE TUBE 2.7ML WITH LIGHT BLUE HEMOGARD CLOSURE

FDA Adverse Event
Malfunction ·BECTON, DICKINSON AND COMPANY (BD)·Product code JKA·December 5, 2017

BD VACUTAINER® PLUS CITRATE TUBE

FDA Adverse Event
Malfunction ·BECTON, DICKINSON AND COMPANY (BD)·Product code JKA·December 1, 2017

BD VACUTAINER® PLUS CITRATE TUBE

FDA Adverse Event
Malfunction ·BECTON, DICKINSON AND COMPANY (BD)·Product code JKA·December 6, 2017

BD VACUTAINER® CITRATE TUBES 4.5 13X75 NA CITRATE (0.105M = 3.2%)

FDA Adverse Event
Malfunction ·BECTON, DICKINSON AND COMPANY (BD)·Product code JKA·November 10, 2017

BD VACUTAINER® PLUS CITRATE TUBE

FDA Adverse Event
Malfunction ·BECTON, DICKINSON AND COMPANY (BD)·Product code JKA·December 14, 2017

BD VACUTAINER® PLUS CITRATE TUBE

FDA Adverse Event
Malfunction ·BECTON, DICKINSON AND COMPANY (BD)·Product code JKA·December 8, 2017

CITRATE TUBE

FDA Adverse Event
Malfunction ·BECTON, DICKINSON AND COMPANY (BD)·Product code JKA·November 27, 2017

DIDECO LILIPUT ECMO M PHISIO

FDA Adverse Event
Other ·SORIN GROUP ITALIA·Product code DTZ·April 20, 2012

OT VERIO IQ METER

FDA Adverse Event
Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·March 21, 2013

ISOFLEX S

FDA Adverse Event
Injury ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code DTB·March 10, 2011

NUCLEUS 24 CHANNEL COCHLEAR IMPLANT SYSTEM

FDA Adverse Event
Malfunction ·COCHLEAR LTD.·Product code MCM·March 14, 2008

BD VACUTAINER® BUFFERED SODIUM CITRATE (9NC) BLOOD COLLECTION TUBES

FDA Adverse Event
Malfunction ·BECTON, DICKINSON & CO. (BROKEN BOW)·Product code JKA·May 24, 2019

METASUL, ALPHA INSERT, II/32

FDA Adverse Event
Injury ·ZIMMER GMBH·Product code KWA·March 15, 2018

METASUL, ALPHA INSERT, II/32

FDA Adverse Event
Injury ·ZIMMER GMBH·Product code KWA·June 25, 2018

DURASUL, ALPHA INSERT, KK/36

FDA Adverse Event
Malfunction ·ZIMMER GMBH·Product code LZO·March 6, 2018

DURASUL, ALPHA INSERT, HOODED, MM/28

FDA Adverse Event
Injury ·ZIMMER GMBH·Product code JDI·May 22, 2018