10,000 results · 19ms · Sources: EU EUDAMED, US FDA

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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