1,060 results · 19ms · Sources: EU EUDAMED, 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·