53 results · 26ms · 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.

MAGICFIL

FDA 510(k)
FDA Class 2 ·Dental

GC Fuji ORTHO™

FDA UDI
Gc America Inc.·14548161331982·FUJI Ortho LC Paste Pak Automix Set SL

GC Fuji ORTHO™

FDA UDI
Gc America Inc.·D0470135711·FUJI Ortho LC Paste Pak Automix Set SL

ACUFEX

FDA UDI
Smith & Nephew, Inc.·03596010091185·ACL CHAMFERING RASP 8 MM, HALF-ROUND

STEVE MADDEN

FDA UDI
FGX INTERNATIONAL INC.·00193033508251·

STEVE MADDEN

FDA UDI
FGX INTERNATIONAL INC.·00193033508268·

STEVE MADDEN

FDA UDI
FGX INTERNATIONAL INC.·00193033508244·

SERONO FOR USE WITH GONAL-F 1200IU MULTI-DOSE ONLY AT 600IU/ML SYRINGE

FDA 510(k)
FDA Class 2 ·General Hospital

ADC QS/IPD WORKSTATION

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

GMK-SPHERE FEMORAL COMPONENT SPHERE CEMENTED SIZE 5+ L

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·January 13, 2023

BD VACUTAINER® PLUS CITRATE TUBE

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

ENDURANT II ABDOMINAL STENT GRAFT SYSTEM

FDA Adverse Event
Death ·MEDTRONIC IRELAND·Product code MIH·March 20, 2013

SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE

FDA Adverse Event
Injury ·BAXTER HEALTHCARE CORPORATION·Product code KDJ·March 10, 2011

SPRINT FIDELIS

FDA Adverse Event
Injury ·MEDTRONIC PUERTO RICO, INC.·Product code LWS·March 10, 2008

GMK-SPHERE FEMORAL COMPONENT SPHERE CEMENTED SIZE 5+

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·December 13, 2021