Description
BD Vacutainer® PPT™ is a closed system allowing separation and storage of undiluted EDTA plasma in the primary blood collection tube. It is intended for the purposes of molecular diagnostic testing.
PPT™ is an evacuated, sterile blood collection tube that contains an inert gel and spray-dried K2EDTA anticoagulant for achieving plasma separation. When the sample-filled tube is subjected to centrifugation, the gel migrates and forms a physical barrier between the plasma and most of the cellular elements. Since the tube uses spray-dried K2EDTA as opposed to liquid additives, the plasma obtained is undiluted.
| Tube Material | Plastic |
| Tube Size | 13x100 mm |
| Draw Volume | 5 mL |
| Closure Type | BD Hemogard™ |
| Closure Color | Pearl White |
| Label | Mylar (transparent) |
| Cell Separator | Yes (Gel) |
| Anticoagulant | K2EDTA |
| Sterilization | Radiation , 10-3 SAL , ISO11137-1 |
- BD White Paper VS8188: Evaluation Of The Effect Of Specimen Handling Conditions In BD Vacutainer® PPT On The Stability Of HIV-1 Viral Load Using Roche Cobas® Ampliprep/ Cobas® Taqman® HIV-1 Test, 2010.
- BD White Paper VS8189: Evaluation of Specimen Handling Conditions in BD Vacutainer® Plasma Preparation Tube HIV-1 Viral Load as Measured by the Abbott RealTime HIV-1 Assay.
- Evaluation of the VACUTAINER® Brand PPT™ Tubes for HCV Viral Load Testing.
- Determination of the Effect of Freezing BD Vacutainer® PPT™ Plasma in situ on Hepatitis C (HCV) Viral Loads as Measured by the Roche COBAS® TaqMan® HCV ASR.
- Determination of the Effect of Freezing BD Vacutainer® PPT™Plasma in situ on Hepatitis B (HBV) Viral Loads Using the Roche COBAS® TaqMan® HBV RUO Assay.
Preparation And Storage
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.
For In Vitro Diagnostics Use.
Documents are subject to revision without notice. Please verify you have the correct revision of the document, and always refer back to BD's eIFU website for the latest and most up to date information.
Refer to manufacturer's instructions for use and related User Manuals and Technical Data Sheets before using this product 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.