2,459 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Amvex Vacuum Regulator
FDA UDI
OHIO MEDICAL, LLC·00628101501563·VR-PP series, VacReg, Ped Int 2Mode 160mmHg, A...
Yingtai
FDA UDI
Changsha Yingtai Instrument Co., Ltd·06976301910383·Incubator is a temperature-controlled device sp...
SILVER PPP MODULE, ITE
FDA 510(k)
FDA Class 1
·Ear, Nose, Throat
SEPRAMESH IP
FDA Adverse Event
Injury
·DAVOL INC., SUB. C.R. BARD, INC. -1213643·Product code FTL·January 5, 2026
ANGEL CENTRIFUGE US (REFURBISHED)
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code ORG·August 24, 2023
OPERA PPP
FDA Adverse Event
Malfunction
·ARJO MED. AB LTD.·Product code FSA·August 5, 2003
OPERA PPP
FDA Adverse Event
Malfunction
·ARJO MED AB LTD.·Product code FSA·July 19, 2004
TEMPO PPP
FDA Adverse Event
Injury
·ARJO MED AB LTD.·Product code FSA·August 23, 2004
OPERA PPP
FDA Adverse Event
Malfunction
·ARJO, LTD.·Product code FSA·July 31, 2002
OPERA PPP
FDA Adverse Event
Malfunction
·ARJO LTD.·Product code FSA·October 30, 2001
TEMPO PPP
FDA Adverse Event
Malfunction
·ARJO MED AB LTD.·Product code FSA·June 25, 2004
TEMPO PPP
FDA Adverse Event
Malfunction
·ARJO MED AB LTD.·Product code FSA·November 13, 2007
OPERA PPP
FDA Adverse Event
Malfunction
·ARJO LTD.·Product code FSA·May 31, 2002
OPERA PPP
FDA Adverse Event
Malfunction
·ARJO, LTD.·Product code FSA·April 23, 2002
OPERA PPP
FDA Adverse Event
Malfunction
·ARJO, LTD.·Product code FSA·May 31, 2002
OPERA PPP
FDA Adverse Event
Malfunction
·ARJO, LTD.·Product code FSA·October 31, 2002
OPERA PPP
FDA Adverse Event
Malfunction
·ARJO LTD.·Product code FSA·October 14, 2002
VICRYL POLYGLACTIN 910 MESH UNKNOWN PRODUCT
FDA Adverse Event
Injury
·ETHICON INC.·Product code FTL·May 3, 2022
ANGEL PRP SYSTEM CENTRIFUGE US (NEW)
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code ORG·April 30, 2024
PROLENE POLYPROPYLENE MESH UNKNOWN PRODUCT
FDA Adverse Event
Injury
·ETHICON INC.·Product code FTL·April 30, 2021