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BD Trucount™ Trucount Absolute Counting Tubes IVD
(IVD)
Regulatory Status Legend
Any use of products other than the permitted use without the express written authorization of Becton, Dickinson and Company is strictly prohibited.
Description | Quantity/Size | Part Number | EntrezGene ID |
---|---|---|---|
BD Trucount tubes (25 tubes) | 50 Tests (2 ea) | 91-0786 | N/A |
Development References (6)
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Brando B, Göhde Jr W, Scarpati B, D'Avanzo G. The vanishing counting bead phenomenon: effect on absolute CD34+ cell counting in phosphate-buffered saline–diluted leukapheresis samples. Cytometry. 2001; 43:154-160. (Biology).
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Centers for Disease Control. Update: universal precautions for prevention of transmission of human immunodeficiency virus, hepatitis B virus, and other bloodborne pathogens in healthcare settings. MMWR. 1988; 37:377-388. (Biology).
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Clinical Applications of Flow Cytometry: Quality Assurance and Immunophenotyping of Lymphocytes: Approved Guideline. NCCLS document H42-A. 1998. (Biology).
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Jackson AL, Warner NL. Rose NR, Friedman H, Fahey JL, ed. Manual of Clincial Laboratory Immunology, Third Edition. Washington DC: American Society for Microbiology; 1986:226-235.
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NCCLS document. 2001. (Biology).
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Procedures for the Collection of Diagnostic Blood Specimens by Venipuncture–Fourth Edition; Approved Standard. NCCLS document H3-A4. 1998. (Biology).
Please refer to Support Documents for Quality Certificates
Global - Refer to manufacturer's instructions for use and related User Manuals and Technical data sheets before using this products as described
Comparisons, where applicable, are made against older BD Technology, manual methods or are general performance claims. Comparisons are not made against non-BD technologies, unless otherwise noted.
BD FACSCanto™ and BD FACSLyric™ Flow Cytometers are Class 1 Laser Products.
The BD FACSCanto™ Flow Cytometer is for In Vitro Diagnostic Use for up to six colors. Seven to ten colors are for Research Use Only.
The BD FACSLyric™ flow cytometer is for In Vitro Diagnostic Use. CE marked in compliance with the European In Vitro Medical Device Directive 98/79/EC
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