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Owren’s Veronal Buffer for coagulation tests and as a rinsing solution for [CA__ SYSTEM] [BUFFER] is ready for use. Bring to room temperature
the sample needles of the Sysmex® CA Systems. (+15 to +25 °C) before use.
Storage and Stability
Summary and Explanation Stored unopened at +2 to +8 °C, [CA__ SYSTEM] [BUFFER] can be used
Owren’s Veronal Buffer was specially developed for coagulation tests but until the labelled expiry date. Do not freeze. Once opened, [CA__ SYSTEM]
can also be used in all situations requiring an isotonic barbital buffer with [BUFFER] is stable for 30 days at room temperature (+15 to +25 °C).
a pH of 7.35.
Test Procedure
Reagents
Instrument-specific details on the use of the Dade® CA System Buffer are
Materials provided given in the instruction manuals for the Sysmex® CA Systems as well as in
[CA__ SYSTEM] [BUFFER], [REF] B4265 the relevant Reference Guides (Application Sheets) provided by Siemens
Healthcare Diagnostics.
4 x 500 mL, [CA__ SYSTEM] [BUFFER], CA System Buffer
Dade is a trademark of Siemens Healthcare Diagnostics.
Composition
Sysmex is a registered trademark of the SYSMEX CORPORATION.
Dade® CA System Buffer: 2.84 x 10-2 M sodium barbital in 1.25 x 10-1 M
sodium chloride solution, pH 7.35 ± 0.1.
Warnings and Precautions
1. For in-vitro diagnostic use only.
2. The pipetting steps must be performed with care in order to avoid con-
Edition May 2008
tamination. Visible turbidity and flocculation are signs of microbial con-
tamination.
3. Not for internal or external use in humans or animals.
Testdurchführung
Diagnostische Bedeutung
Gerätespezifische Angaben zum Gebrauch des Dade® CA System-Puffers
Owren's Veronal-Puffer wurde speziell für Gerinnungsuntersuchungen
sind in der Bedienungsanleitung der Sysmex® CA Systeme enthalten sowie
entwickelt, kann aber auch überall dort eingesetzt werden, wo ein isoto-
in den entsprechenden Referenzhandbüchern (Applikationsvorschriften),
nischer Barbitalpuffer mit pH 7,35 benötigt wird.
die Siemens Healthcare Diagnostics bereitstellt.