10,000 results
·
19ms
·
Sources: EU EUDAMED, US FDA
LGM INTERNATIONAL, INC.
Manufacturer
🇺🇸 United States
LGM INTERNATIONAL INC.
FDA registration
LGM INTERNATIONAL INC.·5 products·🇺🇸 United States
LGM PHARMA SOLUTIONS, LLC
FDA registration
LGM PHARMA SOLUTIONS, LLC·1 product·🇺🇸 United States
KVP
FDA UDI
KVP International, Inc.·00742061700245·KVP Latex Gloves Medium (100 pk)
NEPHELRATE ANTIPERUMS LGM
FDA 510(k)
FDA Class 2
·Immunology
HAV lgM Rapid Test
Device
EU IVDD
·
Eu Ivd General
·Beijing Jinwofu Bioengineering Technology Co., Ltd.·On the market
RAPI/TEX-LGM KIT
FDA 510(k)
FDA Class 2
·Immunology
VENA TECH VENA CAVA FILTER
FDA Adverse Event
Malfunction
·B. BRAUN VENA-TECH·Product code DTK·May 12, 1998
VENATECH
FDA Adverse Event
Death
·B. BRAUN MEDICAL INC.·Product code DTK·July 10, 2008
AMERICAN PROTECTIVE PRODUCTS
FDA UDI
American Protective Products LLC·10850063932599·
ELECSYS 2010
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code JJE·May 17, 2007
INCSTAR EPSTEIN-BARR VIRAL CAPSID ANTIGEN (VCA) LGM ELISA KIT
FDA 510(k)
FDA Class 1
·Microbiology
RapidFor™ SARS-CoV-2 lgG/lgM Test Kit
Device
EU IVDD
·
Eu Ivd General
·Vitrosens Biyoteknoloji Anonim Şirketi·On the market
RapidFor™ SARS-CoV-2 lgG/lgM Test Kit
Device
EU IVDD
·
Eu Ivd General
·Vitrosens Biyoteknoloji Anonim Şirketi·On the market
VENA TECH
FDA Adverse Event
Injury
·B. BRAUN MEDICAL, INC.·Product code DTK·August 19, 2004
ANALYTICAL E MODULE
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code LGD·June 3, 2007
INTEGRA 700
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code JJE·April 4, 2007
VENA TECH - LGM
FDA Adverse Event
Death
·*·Product code DTK·March 2, 2006
VENA TECH-LGM
FDA Adverse Event
Death
·VENA TECH B. BRAUN MEDICAL·Product code DTK·October 1, 1997
VENA TECH VENA CAVA FILTER
FDA Adverse Event
Malfunction
·B. BRAUN VENA-TECH·Product code DTK·April 30, 1998