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Position: Chinese Standard in English/YY/T 0681.9-2011
YY/T 0681.9-2011   Test methods for sterile medical device package—Part 9:Burst testing of flexible package seals using internal air pressurization weight restraining plates (English Version)
Standard No.: YY/T 0681.9-2011 Status:valid remind me the status change

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Standard No.: YY/T 0681.9-2011
English Name: Test methods for sterile medical device package—Part 9:Burst testing of flexible package seals using internal air pressurization weight restraining plates
Chinese Name: 无菌医疗器械包装试验方法 第9部分:约束板内部气压法软包装密封胀破试验
Chinese Classification: C31    General and microsurgical devices
Professional Classification: YY    Professional Standard - Pharmaceutics
Source Content Issued by: China Food and Drug Administration
Issued on: 2011-12-31
Implemented on: 2013-6-1
Status: valid
Target Language: English
File Format: PDF
Word Count: 7000 words
Translation Price(USD): 210.0
Delivery: via email in 1 business day
Test methods for sterile medical device package — Part 9: Burst testing of flexible package seals using internal air pressurization within restraining plates 1 Scope The test method specified in this part of YY/T 0681 specifies the method to inspect the minimum bursting strength at the periphery seal of the flexible package, which is placed in the restraining plate and internally pressurized. This test is only applicable to flexible packages with sealed peripheries (usually referred to pouch). Especially applicable to packaging which seal has peelable characteristics (the contents are taken out after being peeled off by the end user). It is suggested that users of this method pay special attention to the possibility of designing and manufacturing restraining plate clamps. See Informative Annex C for details about pressure factors and structural design considerations. 2 Normative references The following referenced documents are indispensable for the application of this document. For dated references, only the edition cited applies. For undated references, the latest edition of the referenced document (including any amendments) applies. YY/T 0681.2 Test methods for sterile medical device package — Part 2: Seal strength of flexible barrier materials YY/T 0681.3 Test methods for sterile medical device package — Part 3: Internal pressurization failure resistance of unrestrained packages 3 Terms and definitions For the purposes of this standard, the following terms and definitions apply. 3.1 flexible package or pouch package that at least one sealing material on the package is a flexible structure (such as paper, polyethylene, etc.) 3.2 restraining plates rigid plate which contacts and limits the expansion of the package surface when the package is pressurized 4 Summary of test method 4.1 Inflate air pressure into the test package on one apparatus until the package ruptures burst. In most cases, the burst occurs at one or more areas of the seal. Inflating and pressurizing equipment is required to keep the internal pressure increase before the seal is broken. In the process of pressurization, the package shall be placed between two rigid parallel plates (restraining plates) to limit the distension and deformation of the package, but leave the sealed peripheral area unrestrained. A sensor inserted inside the package detects the internal pressure when the package breaks. According to the application situation, this test method needs to use two kinds of restraining plates, which are described as follows: 4.1.1 Open packaging configuration: used for package with three peripheries sealed and the fourth side open. This configuration is often used in the production of preformed packages. See Figure 1 for operating instructions of this configuration. 4.1.2 Closed package configuration: used for package with four sides sealed. This configuration is often used to test the seal of the package in a completely sealed state. See Figure 2 for operating instructions of this configuration. 5 Significance and use 5.1 This test provides a quick assessment method for evaluating the sealing failure trend of package under differential pressure. Differential pressure may occur during the processes of sterilization and transportation. This test method is used to measure the bursting strength of the sealed area of package (i.e., bursting often occurs in one or several sealed areas). The minimum bursting strength value of the sealed area may be very important for the package manufacturer and the end user to ensure proper package integrity. This test method cannot provide a measurement for the uniformity of package seal. This test method cannot be used to evaluate the integrity of the whole package, that is, it cannot evaluate the bursting strength of the contact part between the package and the restraining plate. If necessary, this test method should be used in combination with other assessment methods of the whole package integrity, uniformity of package sealing or opening performance.
Foreword i Introduction ii 1 Scope 2 Normative references 3 Terms and definitions 4 Summary of test method 5 Significance and use 6 Apparatus 7 Sampling 8 Conditioning 9 Procedure 10 Report Annex A (Normative) Recommendations for determining the gap distance between restraining plates Annex B (Informative) Factors influencing test results between laboratories Annex C (Informative) Precision and bias of the test methods Bibliography
Referred in YY/T 0681.9-2011:
*YY/T 0681.2-2010 Test methods for sterile medical device package—Part 2:Seal strength of flexible battier materials
*YY/T 0681.3-2010 Test methods for sterile medical device package—Part 3:Internal pressurization failure resistance of unrestrained packages
Code of China
Standard
YY/T 0681.9-2011  Test methods for sterile medical device package—Part 9:Burst testing of flexible package seals using internal air pressurization weight restraining plates (English Version)
Standard No.YY/T 0681.9-2011
Statusvalid
LanguageEnglish
File FormatPDF
Word Count7000 words
Price(USD)210.0
Implemented on2013-6-1
Deliveryvia email in 1 business day
Detail of YY/T 0681.9-2011
Standard No.
YY/T 0681.9-2011
English Name
Test methods for sterile medical device package—Part 9:Burst testing of flexible package seals using internal air pressurization weight restraining plates
Chinese Name
无菌医疗器械包装试验方法 第9部分:约束板内部气压法软包装密封胀破试验
Chinese Classification
C31
Professional Classification
YY
ICS Classification
Issued by
China Food and Drug Administration
Issued on
2011-12-31
Implemented on
2013-6-1
Status
valid
Superseded by
Superseded on
Abolished on
Superseding
Language
English
File Format
PDF
Word Count
7000 words
Price(USD)
210.0
Keywords
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Introduction of YY/T 0681.9-2011
Test methods for sterile medical device package — Part 9: Burst testing of flexible package seals using internal air pressurization within restraining plates 1 Scope The test method specified in this part of YY/T 0681 specifies the method to inspect the minimum bursting strength at the periphery seal of the flexible package, which is placed in the restraining plate and internally pressurized. This test is only applicable to flexible packages with sealed peripheries (usually referred to pouch). Especially applicable to packaging which seal has peelable characteristics (the contents are taken out after being peeled off by the end user). It is suggested that users of this method pay special attention to the possibility of designing and manufacturing restraining plate clamps. See Informative Annex C for details about pressure factors and structural design considerations. 2 Normative references The following referenced documents are indispensable for the application of this document. For dated references, only the edition cited applies. For undated references, the latest edition of the referenced document (including any amendments) applies. YY/T 0681.2 Test methods for sterile medical device package — Part 2: Seal strength of flexible barrier materials YY/T 0681.3 Test methods for sterile medical device package — Part 3: Internal pressurization failure resistance of unrestrained packages 3 Terms and definitions For the purposes of this standard, the following terms and definitions apply. 3.1 flexible package or pouch package that at least one sealing material on the package is a flexible structure (such as paper, polyethylene, etc.) 3.2 restraining plates rigid plate which contacts and limits the expansion of the package surface when the package is pressurized 4 Summary of test method 4.1 Inflate air pressure into the test package on one apparatus until the package ruptures burst. In most cases, the burst occurs at one or more areas of the seal. Inflating and pressurizing equipment is required to keep the internal pressure increase before the seal is broken. In the process of pressurization, the package shall be placed between two rigid parallel plates (restraining plates) to limit the distension and deformation of the package, but leave the sealed peripheral area unrestrained. A sensor inserted inside the package detects the internal pressure when the package breaks. According to the application situation, this test method needs to use two kinds of restraining plates, which are described as follows: 4.1.1 Open packaging configuration: used for package with three peripheries sealed and the fourth side open. This configuration is often used in the production of preformed packages. See Figure 1 for operating instructions of this configuration. 4.1.2 Closed package configuration: used for package with four sides sealed. This configuration is often used to test the seal of the package in a completely sealed state. See Figure 2 for operating instructions of this configuration. 5 Significance and use 5.1 This test provides a quick assessment method for evaluating the sealing failure trend of package under differential pressure. Differential pressure may occur during the processes of sterilization and transportation. This test method is used to measure the bursting strength of the sealed area of package (i.e., bursting often occurs in one or several sealed areas). The minimum bursting strength value of the sealed area may be very important for the package manufacturer and the end user to ensure proper package integrity. This test method cannot provide a measurement for the uniformity of package seal. This test method cannot be used to evaluate the integrity of the whole package, that is, it cannot evaluate the bursting strength of the contact part between the package and the restraining plate. If necessary, this test method should be used in combination with other assessment methods of the whole package integrity, uniformity of package sealing or opening performance.
Contents of YY/T 0681.9-2011
Foreword i Introduction ii 1 Scope 2 Normative references 3 Terms and definitions 4 Summary of test method 5 Significance and use 6 Apparatus 7 Sampling 8 Conditioning 9 Procedure 10 Report Annex A (Normative) Recommendations for determining the gap distance between restraining plates Annex B (Informative) Factors influencing test results between laboratories Annex C (Informative) Precision and bias of the test methods Bibliography
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