Precinorm HBA1C.12173506001.V13.en

12173506001V13.
Precinorm HBA1C
11488422 122 3 x 1mL Control
03004295 922 3 x 1mL Control (QCS)
English S 24/25 Avoid contact with skin and eyes.

System information Contact phone: all countries: +49-621-7590, USA: +1-800-428-2336
For use on Roche/HitachiMODULAR analyzers the control code is 354. All human material should be considered potentially infectious. All products
Intended use derived from human blood are prepared exclusively from the blood of
donors tested individually and shown to be free from HBsAg and antibodies
PrecinormHBA1C is for use in quality control by monitoring accuracy and to HCV and HIV.
precision for the quantitative methods as specified in the value sheets. The testing methods applied were FDA-approved or cleared in compliance
Summary with the European Directive 98/79/EC, AnnexII, ListA.
PrecinormHBA1C is a lyophilized control based on hemolyzed sheep However, as no testing method can rule out the potential risk of infection
blood. The adjusted concentration of the control components are usually in with absolute certainty, the material should be handled with the same level
the normal range or at the normal/pathological threshold. of care as a patient specimen. In the event of exposure, the directives of the
responsible health authorities should be followed.1,2
Some methods specified in the relevant value sheet may not be available in
all countries. Handling
Carefully open one bottle, avoiding the loss of lyophilizate, and pipette in
Reagents working solutions exactly 1.0mL of distilled/deionized water. Carefully close the bottle and
Reactive components in the lyophilizate: dissolve the contents completely by occasional gentle swirling within
Hemolyzed sheep blood with chemical additives and material of biological 30minutes. Avoid the formation of foam.
origin as specified. The origin of the biological additives is as follows: Do not further hemolyze the ready-for-use controls.
Analyte Origin The enclosed barcoded labels are intended exclusively for the
Roche/HitachiMODULAR analyzers to identify the control. Attach the
Hemoglobin (Hb) sheep blood barcoded labels to the tubes carrying the sample cups containing the
HbA1c human blood control material.
Non-reactive components in the lyophilizate: Storage and stability
Store at 28C.
Preservatives and stabilizers.
Criterion for the stability data stated by Roche:
The concentrations of the components are lotspecific. The exact target
values are given in the enclosed value sheets. Recovery within 10% of initial value.
The values are also encoded in the enclosed control barcode sheets for Stability of the lyophilized control at 28C:
Roche/HitachiMODULAR analyzers. Up to the stated expiration date.
Target values and ranges Stability of components in reconstituted control:
The target values were determined using the method stated in the enclosed
value sheets. Determinations for Roche methods were performed under at 1525C 8hours
strictly standardized conditions on Roche analyzers using Roche system at 28C 7days
reagents and the Roche master calibrator. The target value specified is the
median of all values obtained. The corresponding control range is at (-15)(-25)C 12weeks (when frozen 4times in original
calculated as the target value 3standard deviations (the standard bottle)
deviation being the value obtained from several target value Store control tightly capped when not in use.
determinations). Results should be within the defined ranges. Each
laboratory should establish corrective measures to be taken if values fall Materials provided
outside the range. See Reagents working solutions section
A clinically insignificant difference may be seen between the value(s) listed
on the value sheet and the value(s) obtained from the instrument readable Barcoded labels
data. This is caused by: Materials required (but not provided)
the rounding of value(s) during conversion from the unit in the Roche system reagents and clinical chemistry analyzers
instrument readable data to the unit that is being used. General laboratory equipment
the calculation of the ranges by the analyzer using the percentage Assay
values for the ranges encoded in the barcodes.
Dispense the required volume into a sample cup and analyze in the same
The traceability of the target value is given in the respective Method Sheets way as patient samples.
for the system reagents to be used in combination with the recommended
calibrator. The controls should be run daily in parallel with patient samples and after
every calibration. Control intervals must be adapted to individual
Precautions and warnings laboratorys requirements.
For in vitro diagnostic use. Follow the applicable government regulations and local guidelines for
Exercise the normal precautions required for handling all laboratory quality control.
reagents.
Disposal of all waste material should be in accordance with local guidelines. Limitations-interference
Safety data sheet available for professional user on request. Please note, this QC material does not assess the manual hemolyzing step.
This kit contains components classified as follows in accordance with the References
European directive 1999/45/EC: 1 Occupational Safety and Health Standards: bloodborne pathogens.
(29CFR Part 1910.1030). Fed. Register.
2 Directive 2000/54/EC of the European Parliament and Council of
Xi Irritant (tetradecyltrimethylammonium bromide, 18September 2000 on the protection of workers from risks related to
TTAB) exposure to biological agents at work.
A point (period/stop) is always used in this Method Sheet as the decimal
R 36/38 Irritating to eyes and skin. separator to mark the border between the integral and the fractional parts of
a decimal numeral. Separators for thousands are not used.
2016-05, V 13.0 English 1/2

12173506001V13.0
Precinorm HBA1C
Symbols
Roche Diagnostics uses the following symbols and signs in addition to
those listed in the ISO 152231 standard.
Contents of kit
Volume after reconstitution or mixing
FOR US CUSTOMERS ONLY: LIMITED WARRANTY

Roche Diagnostics warrants that this product will meet the specifications
stated in the labeling when used in accordance with such labeling and will
be free from defects in material and workmanship until the expiration date
printed on the label. THIS LIMITED WARRANTY IS IN LIEU OF ANY
OTHER WARRANTY, EXPRESS OR IMPLIED, INCLUDING ANY IMPLIED
WARRANTY OF MERCHANTABILITY OR FITNESS FOR PARTICULAR
PURPOSE. IN NO EVENT SHALL ROCHE DIAGNOSTICS BE LIABLE
FOR INCIDENTAL, INDIRECT, SPECIAL OR CONSEQUENTIAL
DAMAGES.
COBAS, MODULAR and PRECINORM are trademarks of Roche.
All other product names and trademarks are the property of their respective owners.
Significant additions or changes are indicated by a change bar in the margin.
2013, Roche Diagnostics
Roche Diagnostics GmbH, SandhoferStrasse116, D-68305 Mannheim

www.roche.com
Distribution in USA by:
Roche Diagnostics, Indianapolis, IN
US Customer Technical Support 1-800-428-2336
2/2 2016-05, V 13.0 English

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12173506001V13.

English S 24/25 Avoid contact with skin and eyes.

2016-05, V 13.0 English 1/2

FOR US CUSTOMERS ONLY: LIMITED WARRANTY

Roche Diagnostics GmbH, SandhoferStrasse116, D-68305 Mannheim

2/2 2016-05, V 13.0 English

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