Powered by Google www.ChineseStandard.net Database: 189759 (14 Jul 2024)

YY/T 0681.13-2014 PDF in English


YY/T 0681.13-2014 (YY/T0681.13-2014, YYT 0681.13-2014, YYT0681.13-2014)
Standard IDContents [version]USDSTEP2[PDF] delivered inName of Chinese StandardStatus
YY/T 0681.13-2014English175 Add to Cart 0-9 seconds. Auto-delivery. Test methods for sterile medical device package. Part 13: Slow rate penetration resistance of flexible barrier films and laminates Valid

PDF Preview

Standards related to: YY/T 0681.13-2014

YY/T 0681.13-2014: PDF in English (YYT 0681.13-2014)

YY/T 0681.13-2014
PHARMACEUTICAL INDUSTRY STANDARD
OF THE PEOPLE’S REPUBLIC OF CHINA
ICS 11.080.040
C 31
Test methods for sterile medical device package -
Part 13: Slow rate penetration resistance of flexible
barrier films and laminates
ISSUED ON: JUNE 17, 2014
IMPLEMENTED ON: JULY 01, 2015
Issued by: China Food and Drug Administration
Table of Contents
Foreword ... 3 
1 Scope ... 5 
2 Normative references ... 5 
3 Terminology ... 5 
4 Significance and application ... 6 
5 Instruments ... 6 
6 Specimen ... 7 
7 Instrument preparation ... 8 
8 Number of specimens ... 8 
9 State conditioning ... 8 
10 Procedure ... 8 
11 Report ... 9 
Appendix A (Informative) Precision and bias ... 11 
Foreword
YY/T 0681 “Test methods for sterile medical device package” is divided into the
following parts:
- Part 1: Test guide for accelerated aging;
- Part 2: Seal strength of flexible battier materials;
- Part 3: Internal pressurization failure resistance of unrestrained packages;
- Part 4: Detecting seal leaks in porous packages by dye penetration;
- Part 5: Detecting gross leaks in medical packaging by internal
pressurization (bubble test)
- Part 6: Evaluation of chemical resistance of printed inks and coatings on
flexible packaging materials;
- Part 7: Evaluating inks or coating adhesion to flexible packaging materials
using tape;
- Part 8: Coating/adhesive weight determination;
- Part 9: Burst testing of flexible package seals using internal air
pressurization weight restraining plates;
- Part 10: Test for microbial barrier ranking of porous package material;
- Part 11: Determining integrity of seals for medical packaging by visual
inspection;
- Part 12: Flex durability of flexible barrier films;
- Part 13: Slow rate penetration resistance of flexible barrier films and
laminates.
This part is Part 13 of YY/T 0681.
This part was drafted in accordance with the rules given in GB/T 1.1-2009.
This part was formulated with reference to ASTM F1306-1990 "Slow rate
penetration resistance of flexible barrier films and laminates".
Please note that some elements of this document may involve patents. The
issuer of this document is not responsible for identifying these patents.
This part shall be under the jurisdiction of the National Technical Committee for
Test methods for sterile medical device package -
Part 13: Slow rate penetration resistance of flexible
barrier films and laminates
1 Scope
This part of YY/T 0681 is applicable to determine the penetration resistance of
the anti-drive probe of flexible barrier film and laminates. In this test, biaxial
stress is applied to the material at a constant test rate at room temperature,
until penetration occurs; the force, energy and elongation before penetration
are measured.
Note: Appendix A gives the precision and bias of the test methods as specified in this
part.
2 Normative references
The following documents are essential to the application of this document. For
the dated documents, only the versions with the dates indicated are applicable
to this document; for the undated documents, only the latest version (including
all the amendments) are applicable to this standard.
GB/T 2918 Plastics - Standard atmospheres for conditioning and testing
(GB/T 2918-1998, idt ISO 291:1997)
3 Terminology
The following terms and definitions apply to this document.
3.1
Elongation
The elastic / plastic deformation of the driving probe when it penetrates the
flexible film.
3.2
Penetration resistance
6.2 The specimen size shall be 76 mm × 76 mm.
7 Instrument preparation
7.1 Set up and operate the instrument according to the instrument’s operation
manual.
7.2 Install the probe.
7.3 Place the probe above the clamp and align it.
8 Number of specimens
Test at least 5 specimens for each sample.
9 State conditioning
9.1 According to the provisions of GB/T 2918 before the test, condition the state
of the specimen under the conditions of temperature (23 ± 2) °C and relative
humidity (50 ± 5) % for at least 40 h.
9.2 Unless otherwise specified in this test method, the test is performed under
standard laboratory conditions with a temperature of (23 ± 2) °C and a relative
humidity of (50 ± 5) %.
10 Procedure
10.1 Calibrate the test instrument according to the instrument manufacturer's
instructions.
10.2 Select the force of the dynamometer in the range of 20% ~ 80% of the
range when penetration occurs.
10.3 Use the sample cutter to cut at least five 76 mm × 76 mm specimens for
each sample.
10.4 Measure the thickness in the center of the film sample (average of 3
readings).
Note 1: The thickness can be measured by ASTM D374 or GB/T 6672. It is
recommended to use Method C or Method D of ASTM D374 first.
Note 2: The accuracy of the thickness measurement methods in Table A.3 is based on
ASTM D374.
Appendix A
(Informative)
Precision and bias
A.1 Precision
A.1.1 Precision data
Table A.1 and Table A.2 are the research results of laboratory collaborative tests
conducted by ASTM on six materials in accordance with ASTM E691 in six
laboratories from 1988 to 1989. All samples of each material came from the
same source, but the specimens were prepared in each participating laboratory.
Each test result is an independently measured test value. Each laboratory
obtained 5 test results for each material. Each laboratory conducted two parallel
tests on each material; treated them as independent materials.
Tables A.3 and A.4 are based on the collaborative tests of the above
laboratories. But the data is from 3 laboratories and 4 laboratories, respectively.
When using it, it should pay attention to the relatively small amount of data.
Note: The following (A.1.2) explanation of r and R is only intended to give the concept
of the approximate precision of this test method. Tables A.1 and A.3 should not be
strictly used for the acceptance or rejection of materials, because these data are only
for the materials involved in the verification, but do not represent other batches,
conditions, materials or laboratories. Users of this test method should obtain data for
specific laboratories and materials or between specific laboratories. An explanation of
these data is given in A.1.2.
A.1.2 Concepts of r and R
A.1.2.1 If Sr is obtained from enough data, the difference between the two test
results obtained by the same operator, using the same equipment, and on the
same day exceeds the repeatability limit (r) of the material, it should be
determined that the two test results are not equivalent.
A.1.2.2 If the SR is obtained from sufficient data, the two test results obtained
by different operators, using different equipment, and in different laboratories
for the same material exceed the material reproducibility limit (R ), it should be
determined that the two test results are not equivalent.
A.1.2.3 For the judgement according to A.1.2.1 and A.1.2.2, the correct
probability is about 95% (0.95).
A.2 Bias
......
 
Source: Above contents are excerpted from the PDF -- translated/reviewed by: www.chinesestandard.net / Wayne Zheng et al.