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  • Dispositivo 1149
  • Fabricante 31827
  • Evento 1201
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Nombre Clasificación Fabricante Nivel de riesgo País Fuente
Zoll Medical Immunology and Microbiology Devices Zoll Medical Corporation 3 United States USFDA
Xpert Infinity Software Immunology and Microbiology Devices Cepheid 1 United States USFDA
Xpert GBS Immunology and Microbiology Devices Cepheid 1 United States USFDA
Xpert CT/NG Immunology and Microbiology Devices Cepheid 2 United States USFDA
Xpect Giardia/Cryptosporidium Kit Immunology and Microbiology Devices Remel, Inc 2 United States USFDA
West Nile Virus IgM Capture ELISA Immunology and Microbiology Devices Inverness Medical 2 United States USFDA
West Nile Virus IgG DxSelect Immunology and Microbiology Devices Focus Diagnostics Inc 2 United States USFDA
WELCH ALLYN PIC 50 Immunology and Microbiology Devices ROXON MEDI-TECH LTD. Canada HC
WASP (Walk Away Specimen Process) Instrument software Immunology and Microbiology Devices Copan Italia 1 United States USFDA
Vitros Immunodiagnostic Products CEA REAGENT PACK, Lot 750, REF 192 0115, 100 coated wells per pack. Firm on the label: Ortho-Clinical Diagnostics, Amersham, UK. Immunology and Microbiology Devices Ortho-Clinical Diagnostics 2 United States USFDA
VITROS Immunodiagnostic Products CA 19-9 Calibrators and Reagent Packs An in vitro diagnostic medical device (IVD) Immunology and Microbiology Devices Ortho-Clinical Diagnostics Australia DHTGA
VITROS Immunodiagnostic Products CA 125 II Calibrators Immunology and Microbiology Devices Ortho-Clinical Diagnostics 2 United States USFDA
VITROS Immunodiagnostic Products AntiHCV Reagent Pack Immunology and Microbiology Devices ORTHO-CLINICAL DIAGNOSTICS 3 United States USFDA
VITROS Immunodiagnostic Products AntiHBs Calibrators & AntiHBs Reagent Packs Immunology and Microbiology Devices Ortho-Clinical Diagnostics 3 United States USFDA
Vitros Immunodiagnostic HBsAg CONFIRMATORY KIT * REF 680 1324. Firm on label: Ortho-Clinical Diagnostics, 62 The Broadway, Amersham, Bucks, UK. UPC *+H221680132412* . Each kit contains: 1 x kit of reagents, and protocol card for HBsAg Confirmatory Kit. According to the firm (but not on label), there are 60 neutralization reactions per confirmatory kit. Immunology and Microbiology Devices Ortho-Clinical Diagnostics 3 United States USFDA
VITROS CRP Slides: (1) Cat # 192 6740, 250 slides per box, and (2) Cat # 809 7990, 90 slides per box. Firm on the label: Ortho-Clinical Diagnostics, Inc., Rochester, NY 14626. The CRP Slides are for use on the Vitros 250/250AT and/or Vitros 950/950AT Clinical Chemistry Systems. For in vitro diagnostic use. Vitros CRP slides quantitatively measure C-reactive protein concentration in serum and plasma. Immunology and Microbiology Devices Ortho-Clinical Diagnostics 2 United States USFDA
Vitros CRP (C-Reactive Protein) Slides. Catalog #192 6740 contains 250 slides; Catalog #809 7990 contains 90 slides. Firm on label: Ortho-Clinical Diagnostics, a Johnson & Johnson Company, Rochester, NY 14626. Immunology and Microbiology Devices Ortho-Clinical Diagnostics 2 United States USFDA
VITROS Chemistry Products CRP Slides Immunology and Microbiology Devices Ortho-Clinical Diagnostics 2 United States USFDA
VITEK GPS107 Gram Positive Susceptibility Card Immunology and Microbiology Devices bioMerieux Inc 2 United States USFDA
VITEK GPS107 Gram Positive Susceptibility Card Immunology and Microbiology Devices bioMerieux Inc 2 United States USFDA
Vitek 2 YST ID Immunology and Microbiology Devices Biomerieux Inc 1 United States USFDA
Vitek 2 NH ID Immunology and Microbiology Devices Biomerieux Inc 1 United States USFDA
Vitek 2 Gram Positive Susceptibility Test Cards Immunology and Microbiology Devices Biomerieux Hong Kong DH
VITEK 2 Gram Positive Antimicrobial Susceptibility Testing (AST) Cards Immunology and Microbiology Devices BioMerieux Hong Kong DH
VITEK 2 Gram Negative Susceptibility Card, ASTN184 Immunology and Microbiology Devices Biomerieux Inc 2 United States USFDA
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Los dispositivos médicos ayudan con el diagnóstico, la prevención y el tratamiento de muchas lesiones y enfermedades. A través de la International Medical Devices Database no estamos sugiriendo que compañías u otras entidades mencionadas en la base de datos hayan sido parte de una conducta ilegal o hayan actuado de manera impropia. Un mismo dispositivo médico puede tener distintos nombres en diferentes países. Esta base de datos no busca proporcionar asesoría médica. Los pacientes deben consultar con sus médicos para determinar si la data contiene información relevante y si la misma tiene implicaciones médicas para ellos.