1,060 results
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19ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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REFLEX CATHETER
FDA Adverse Event
Death
·MICRO THERAPEUTICS, INC. DBA EV3·Product code DQY·March 18, 2025
BARDPORT IMPLANTED PORT
FDA Adverse Event
Injury
·BARD ACCESS SYSTEMS·Product code LJY·November 14, 1996
VIDAS® MUMPS IGG ASSAY
FDA Adverse Event
Malfunction
·BIOMERIEUX SA·Product code LJY·January 13, 2016
VIDAS® MUMPS IGG
FDA Adverse Event
Malfunction
·BIOMERIEUX SA·Product code LJY·February 24, 2016
VIDAS® MUMPS IGG ASSAY
FDA Adverse Event
Malfunction
·BIOMERIEUX SA·Product code LJY·January 13, 2016
VIDAS® MUMPS IGG ASSAY
FDA Adverse Event
Malfunction
·BIOMERIEUX, SA·Product code LJY·February 21, 2018
PROGRAMMING SOFTWARE
FDA Adverse Event
Malfunction
·CYBERONICS - HOUSTON·Product code LJY·May 19, 2016
PROGRAMMING SOFTWARE
FDA Adverse Event
Malfunction
·CYBERONICS - HOUSTON·Product code LJY·May 16, 2016
The ETI-Mumps IgG Enzyme Immunoassay Test Kit is sold with assay software version 1.0. that is designed to work exclusively with the ETI-Max 3000 automated platform (version 1.51.1).
FDA Recall
Terminated
·Diasorin Inc.·Product code LJY·August 8, 2005
AtheNA Multi-Lyte MMV Test System- A93111G A microparticle-based immunoassay intended for the qualitative presumptive detection of IgG class antibody to the Mumps virus in human serum using the AtheNA Multi-Lyte Test System. The test system is intended to be used for determination of a previous infection with the Mumps virus.
FDA Recall
Terminated
·Zeus Scientific, Inc.·Product code LJY·March 8, 2012
Diamedix Is-Mumps IgG Test Kit Diamedix Is-Mumps IgG Test Kit is an EIA procedure intended for the qualitative and semi-quantitative detection of Mumps IgG antibodies as an aid in the diagnosis of Mumps infection.
FDA Recall
Terminated
·Diamedix Corporation·Product code LJY·October 20, 2014
Diamedix Is-Mumps IgG Enzyme Immunoassay Test Kit for In Vitro Diagnostic Use Catalog No. 720-540
FDA Recall
Terminated
·Diamedix Corporation·Product code LJY·January 5, 2018
VIDAS Mumps IgG (MPG), REF 30218
FDA Recall
Open, Classified
·bioMerieux, Inc.·Product code LJY·September 22, 2021
Mumps IgM ELISA 96 Well Kit, Catalog Number: MP060G The products in question are all Enzyme Linked Immunosorbent Assay (ELISA) Test kits designed and marketed for Research Use Only.
FDA Recall
Terminated
·Calbiotech Inc·Product code LJY·August 27, 2008
Plastic bottle containing 3.5 mL of IgG FITC Conjugate Product Usage: Product is a used as a counterstain for various indirect fluorescent assay kits
FDA Recall
Terminated
·Bion Enterprises Ltd·Product code LJY·January 23, 2013
Enzyme Linked Immunoabsorbent Assay, Mumps Virus
FDA classification
FDA Class 1
·Enzyme Linked Immunoabsorbent Assay, Mumps Virus
CJI LTD.
FDA registration
CJI LTD.·5 products·🇹🇼 Taiwan
HJY SMART MEDICAL DEVICE CO., LTD.
FDA registration
HJY SMART MEDICAL DEVICE CO., LTD.·3 products·🇹🇼 Taiwan
LCY .3MM SPOOL
FDA UDI
IVOCLAR VIVADENT, INC.·D7075841360·
LCY .5MM SPOOL
FDA UDI
IVOCLAR VIVADENT, INC.·D7075841410·