36 results
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29ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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DUET SYSTEM
FDA 510(k)
FDA Class 2
·Immunology
LINK Instruments - Chisel, bone curette, raspatory, rongeur
FDA UDI
WALDEMAR LINK GmbH & Co. KG·04026575033805·Orthopaedic prosthesis instrument, reusable - G...
AUTO I.D. JO-1, SCL-70 & PCNA POSITIVE CONTROL SERUM
FDA 510(k)
FDA Class 2
·Immunology
BD INTIMA II CLOSED IV CATHETER
FDA 510(k)
FDA Class 2
·General Hospital
3.5FR URETHANE UMB CATH
FDA Adverse Event
Malfunction
·COVIDIEN MANUFACTURING SOLUTIONS SA·Product code FOS·September 9, 2014
1.9F ARGYLE SINGLE LUMEN PICC
FDA Adverse Event
Malfunction
·COVIDIEN·Product code LJS·September 18, 2014
3.5FR P.U.R. UMBIL CATH X10
FDA Adverse Event
Malfunction
·COVIDIEN·Product code FOS·June 3, 2014
2.5FR URETHANE UMB CATH
FDA Adverse Event
Malfunction
·COVIDIEN·Product code FOS·May 29, 2014
3.5FR URETHANE UMBCATH
FDA Adverse Event
Malfunction
·COVIDIEN·Product code FOS·June 17, 2014
2.5FR URETHANE UMB CATH
FDA Adverse Event
Malfunction
·COVIDIEN·Product code FOS·May 29, 2014
3.5FR P.U.R. UMBIL CATH X10
FDA Adverse Event
Malfunction
·COVIDIEN·Product code FOS·November 7, 2014
3.5FR P.U.R. UMBIL CATH X10
FDA Adverse Event
Malfunction
·COVIDIEN·Product code FOS·October 3, 2014
3.5 FR URETHANE UMB CATH
FDA Adverse Event
Malfunction
·COVIDIEN·Product code FOS·July 28, 2014
DUAL LUMEN INSERTION TRAY
FDA Adverse Event
Malfunction
·COVIDIEN, COVIDIEN MANUFACTURING·Product code LJS·September 18, 2014
DUAL LUMEN INSERTION TRAY
FDA Adverse Event
Malfunction
·COVIDIEN, COVIDIEN MANUFACTURING·Product code LJS·September 18, 2014
3.5FR URETHANE UMB CATH
FDA Adverse Event
Malfunction
·COVIDIEN·Product code FOS·August 22, 2014
3.5FR URETHANE UMB CATH
FDA Adverse Event
Malfunction
·COVIDIEN·Product code FOS·October 20, 2014
3.5FR DUAL-LUMEN UVC CATH
FDA Adverse Event
Malfunction
·COVIDIEN·Product code FOS·October 20, 2014
3.5FR P.U.R. UMBIL CATH X10
FDA Adverse Event
Malfunction
·COVIDIEN·Product code FOS·February 4, 2015
DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Injury
·DEXCOM, INC.·Product code QBJ·April 14, 2026