37 results
·
28ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
HICUT HIGHSPEED INSTRUMENT
FDA 510(k)
FDA Class 2
·Neurology
Gyrus ACMI
FDA UDI
Gyrus ACMI, LLC·00821925034150·SHAPLEIGH WAX CURETTE SMALL, DISPOSABLE (6/PK)
OsteoMed
FDA UDI
OSTEOMED LLC·00845694045131·PrimaLIF LLIF PEEK Implant, 7mm X 22mm X 55mm, ...
TAPERLOC COMPLETE, SIZE 5 AND 6
FDA 510(k)
FDA Class 3
·Orthopedic
ACON BUP ONE STEP BUPRENORPHINE TEST STRIP
FDA 510(k)
FDA Class 2
·Clinical Toxicology
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