23 results
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22ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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CooperSurgical Advincula Delineator Uterine Manipulator
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
BD VACUTAINER® SST¿ BLOOD COLLECTION TUBES
FDA Adverse Event
Injury
·BECTON, DICKINSON & CO., (BD)·Product code JKA·November 21, 2019
ORTHOFIX SCREW
FDA 510(k)
FDA Class 2
·Dental
NON-STERILE, POWDER-FREE, BLUE LATEX EXAMINATION GLOVES, WITHOUT BUBBLE GUM OR GRAPE SCENT,W/ PROTEIN CONTENT CLAIM
FDA 510(k)
FDA Class 1
·General Hospital
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172973936·UniTip High Resolution Catheter 14F
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172970959·
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172970935·
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172970942·
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172970911·
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172973028·
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172973806·
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172973240·
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172970966·
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172970928·
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172970973·
PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP
FDA Adverse Event
Injury
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·June 3, 2013
OT PING METER
FDA Adverse Event
Malfunction
·LIFESCAN INC.·Product code NBW·June 29, 2011
SROM STM ST,36+6L NK,11X16X150
FDA Adverse Event
Injury
·DEPUY-CORK, A DIVISION OF DEPUY ORTHOPAEDICS·Product code MRA·August 28, 2008
INTIMA II¿ CLOSED IV CATHETER SYSTEM
FDA Adverse Event
Malfunction
·BD (SUZHOU)·Product code FOZ·October 31, 2018
BD VACUTAINER® SST¿ BLOOD COLLECTION TUBES
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO., (BD)·Product code JKA·February 10, 2020