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Antisera, Fluorescent, Adenovirus 1-33

FDA product code GNY · Class 1 · Microbiology

42
Registered devices
1
Adverse events
0
Recalls
4
510(k) clearances

Devices with this code

Anti-Adenovirus IFA (IgG) — EUROIMMUN Medizinische Labordiagnostika AGLight Diagnostics ™ Respiratory Screen DFA Reagent — EMD Millipore CorporationAdenovirus IgG Control — Bion Enterprises, Ltd.D3 Fastpoint — DIAGNOSTIC HYBRIDS, INC.Light Diagnostics ™ Adenovirus FITC-Labeled Monoclonal Antibody — EMD Millipore CorporationAdenovirus Antigen (stool) ELISA — DRG International IncLight Diagnostics™ Respiratory Viral Screen IFA Kit — EMD Millipore CorporationAnti-Adenovirus IFA (IgM) — EUROIMMUN Medizinische Labordiagnostika AGD3 Fastpoint — DIAGNOSTIC HYBRIDS, INC.Anti-Adenovirus IFA (IgM) — EUROIMMUN Medizinische Labordiagnostika AGLight Diagnostics ™ Adenovirus Control Slide — EMD Millipore CorporationLight Diagnostics ™ SimulFluor® Respiratory Screen Reagent — EMD Millipore CorporationNovaLisa Adenovirus IgG — Gold Standard Diagnostics Frankfurt GmbHD3 Fastpoint — DIAGNOSTIC HYBRIDS, INC.Light Diagnostics ™ Respiratory Screen DFA Reagent — EMD Millipore CorporationLight Diagnostics™ Respiratory Panel DFA Kit — EMD Millipore CorporationAdenovirus Antigen (stool) ELISA — DRG Instruments Gesellschaft mit beschränkter HaftungLight Diagnostics™ Respiratory Panel Viral Screening and Identification DFA Kit — EMD Millipore CorporationLight Diagnostics ™ Respiratory Viral Screen — EMD Millipore CorporationLight Diagnostics™ Adenovirus DFA Kit — EMD Millipore CorporationLight Diagnostics ™ Adenovirus Control Slides — EMD Millipore CorporationAnti-Adenovirus IFA (IgM) — EUROIMMUN Medizinische Labordiagnostika AGLight Diagnostics ™ Respiratory Viral Control Slides (8 Well) — EMD Millipore CorporationD3 Fastpoint — DIAGNOSTIC HYBRIDS, INC.

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Sourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.