34 results
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22ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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Nitrile Examination Glove Sterile Tested for use with Chemotherapy Drugs Claim, White
FDA 510(k)
FDA Class 1
·General Hospital
RZ Medizintechnik GmbH
FDA UDI
RZ-Medizintechnik GmbH·04049197530309·Tebbet Breast Retractor
190x25...
OCULUS MICROCYN WOUND GEL
FDA 510(k)
FDA Unclassified
·Unknown
MODIFIED ARGYLE POLYURETHANE UMBILICAL VESSEL CATHETER 2.5FR, 3.5FR, 5 FR.
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
5.0FR URETHANE UMB CATH
FDA Adverse Event
Malfunction
·COVIDIEN·Product code FOS·October 31, 2014