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    ASTM F2097 - 14

    Standard Guide for Design and Evaluation of Primary Flexible Packaging for Medical Products

    Active Standard ASTM F2097 | Developed by Subcommittee: F02.50

    Book of Standards Volume: 15.10

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    Significance and Use

    4.1 This design and evaluation guide describes multiple categories for evaluating flexible medical packages and packaging materials. These include safety, barrier properties, durability, package and seal integrity, visibility and appearance, processing, printing ink properties, and package performance.

    4.2 The intent of this design and evaluation guide is to evaluate all cited categories and select those that are applicable. Once the product has been characterized and the sterilization methodology has been defined, there are numerous sets of requirements for any specific package. This design and evaluation guide provides an avenue for assessing these requirements and choosing test methods for both evaluating the package design and monitoring package compliance.

    Note 1Many of the standards included in this guide are consensus standards that are recognized by the United States Food and Drug Administration (FDA). Selection and use of a U.S. FDA recognized consensus standard is voluntary and the sole responsibility of the user in determining its applicability. For further information, consult the U.S. FDA Medical Device Standards Program at

    4.3 Product characterization shall include mass or weight, geometry (length and width, height, and shape) and product composition.

    4.4  All categories must be considered for applicability.

    4.5 The Summary of Test Methods for Medical Packaging Design and Evaluation (Fig. 1) provides a compact graphical presentation of the test methods referenced in this guide.

    4.6 Test Description and Applicability (see Table 1):

    4.6.1 Table 1 lists the test methods commonly used to evaluate flexible medical packaging. The test methods are used in two phases. Package Design: Characterization of the Materials and Evaluation of the Resultant Package—This is referred to as “R&D Evaluation” in Table 1. Testing during this phase is characterized by the generation of quantitative data on the performance of the component materials and the package assembly. These test methods are lengthy, making them inappropriate for the manufacturing environment where rapid response is required for process control. Often, they are expensive and require specialized equipment not readily available at a medical packaging or device manufacturing facility. Package Compliance: Routine Monitoring of Adherence to Specifications—This is referred to as “Compliance Testing” in Table 1. Testing during this phase must be rapid, inexpensive, and readily implemented in a manufacturing environment. The objective is not to develop design data, but to ensure that the design specifications are being met. These test methods do not necessarily make direct measurements of critical values, but detect variations in material, process, or product that are indicative of all critical characteristics.

    4.6.2 It is important to note that no individual test method is entirely predictive of final package performance. Filled packages must be evaluated under conditions of use.

    4.7 Once the design of the package and/or packaging materials has been determined, it may be appropriate to create a package and/or material specification. Guides F99 or F2559 may provide useful guidance.

    1. Scope

    1.1 This guide provides directions for the design and evaluation of primary flexible packages for medical products. The package materials must be selected appropriately for manufacturing process, end use, and the product being packaged.

    1.2 This guide provides a compendium of test methods, practices, and procedures. Specific individual test methods must be selected based on the pertinent characteristics of the specific product to be packaged and the purpose for testing, research and development, or compliance. Not all test methods will be applicable.

    1.3 This guide does not address acceptability criteria, which need to be determined jointly by the package producer and the medical products manufacturer.

    1.4 This guide does not assess the product to be packaged or the sterilization method to be used.

    1.5 The units cited in the referenced standard should be used.

    2. Referenced Documents (purchase separately) The documents listed below are referenced within the subject standard but are not provided as part of the standard.

    ASTM Standards

    D374 Test Methods for Thickness of Solid Electrical Insulation

    D589 Test Method for Opacity of Paper (15 Diffuse Illuminant A, 89 % Reflectance Backing and Paper Backing)

    D638 Test Method for Tensile Properties of Plastics

    D645/D645M Test Method for Thickness of Paper and Paperboard

    D726 Test Method for Resistance of Nonporous Paper to Passage of Air

    D882 Test Method for Tensile Properties of Thin Plastic Sheeting

    D1003 Test Method for Haze and Luminous Transmittance of Transparent Plastics

    D1434 Test Method for Determining Gas Permeability Characteristics of Plastic Film and Sheeting

    D1709 Test Methods for Impact Resistance of Plastic Film by the Free-Falling Dart Method

    D1777 Test Method for Thickness of Textile Materials

    D1894 Test Method for Static and Kinetic Coefficients of Friction of Plastic Film and Sheeting

    D1922 Test Method for Propagation Tear Resistance of Plastic Film and Thin Sheeting by Pendulum Method

    D1938 Test Method for Tear-Propagation Resistance (Trouser Tear) of Plastic Film and Thin Sheeting by a Single-Tear Method

    D2019 Test Method for Dirt in Paper and Paperboard

    D4332 Practice for Conditioning Containers, Packages, or Packaging Components for Testing

    D4754 Test Method for Two-Sided Liquid Extraction of Plastic Materials Using FDA Migration Cell

    F99 Guide for Writing a Specification for Flexible Barrier Rollstock Materials

    F151 Test Method for Residual Solvents in Flexible Barrier Materials

    F372 Test Method for Water Vapor Transmission Rate of Flexible Barrier Materials Using an Infrared Detection Technique

    F895 Test Method for Agar Diffusion Cell Culture Screening for Cytotoxicity

    F904 Test Method for Comparison of Bond Strength or Ply Adhesion of Similar Laminates Made from Flexible Materials

    F1140 Test Methods for Internal Pressurization Failure Resistance of Unrestrained Packages

    F1249 Test Method for Water Vapor Transmission Rate Through Plastic Film and Sheeting Using a Modulated Infrared Sensor

    F1306 Test Method for Slow Rate Penetration Resistance of Flexible Barrier Films and Laminates

    F1307 Test Method for Oxygen Transmission Rate Through Dry Packages Using a Coulometric Sensor

    F1443 Practice for Using 0.008-in. (0.203-mm) Aperture Reflectometers as Test Instruments for Measuring Visual Image Quality of Business Copy Images

    F1608 Test Method for Microbial Ranking of Porous Packaging Materials (Exposure Chamber Method)

    F1884 Test Methods for Determining Residual Solvents in Packaging Materials

    F1886 Test Method for Determining Integrity of Seals for Medical Packaging by Visual Inspection

    F1921 Test Methods for Hot Seal Strength (Hot Tack) of Thermoplastic Polymers and Blends Comprising the Sealing Surfaces of Flexible Webs

    F1927 Test Method for Determination of Oxygen Gas Transmission Rate, Permeability and Permeance at Controlled Relative Humidity Through Barrier Materials Using a Coulometric Detector

    F1929 Test Method for Detecting Seal Leaks in Porous Medical Packaging by Dye Penetration

    F1980 Guide for Accelerated Aging of Sterile Barrier Systems for Medical Devices

    F2029 Practices for Making Heatseals for Determination of Heatsealability of Flexible Webs as Measured by Seal Strength

    F2054 Test Method for Burst Testing of Flexible Package Seals Using Internal Air Pressurization Within Restraining Plates

    F2095 Test Methods for Pressure Decay Leak Test for Flexible Packages With and Without Restraining Plates

    F2096 Test Method for Detecting Gross Leaks in Packaging by Internal Pressurization (Bubble Test)

    F2203 Test Method for Linear Measurement Using Precision Steel Rule

    F2217 Practice for Coating/Adhesive Weight Determination

    F2227 Test Method for Non-Destructive Detection of Leaks in Non-sealed and Empty Packaging Trays by CO2 Tracer Gas Method

    F2228 Test Method for Non-Destructive Detection of Leaks in Packaging Which Incorporates Porous Barrier Material by CO2 Tracer Gas Method

    F2250 Practice for Evaluation of Chemical Resistance of Printed Inks and Coatings on Flexible Packaging Materials

    F2251 Test Method for Thickness Measurement of Flexible Packaging Material

    F2252 Practice for Evaluating Ink or Coating Adhesion to Flexible Packaging Materials Using Tape

    F2338 Test Method for Nondestructive Detection of Leaks in Packages by Vacuum Decay Method

    F2391 Test Method for Measuring Package and Seal Integrity Using Helium as the Tracer Gas

    F2475 Guide for Biocompatibility Evaluation of Medical Device Packaging Materials

    F2476 Test Method for the Determination of Carbon Dioxide Gas Transmission Rate (CO2TR) Through Barrier Materials Using An Infrared Detector

    F2559 Guide for Writing a Specification for Sterilizable Peel Pouches

    F2622 Test Method for Oxygen Gas Transmission Rate Through Plastic Film and Sheeting Using Various Sensors

    F2638 Test Method for Using Aerosol Filtration for Measuring the Performance of Porous Packaging Materials as a Surrogate Microbial Barrier

    F2714 Test Method for Oxygen Headspace Analysis of Packages Using Fluorescent Decay

    F2824 Test Method for Mechanical Seal Strength Testing for Round Cups and Bowl Containers with Flexible Peelable Lids

    F2825 Practice for Climatic Stressing of Packaging Systems for Single Parcel Delivery

    F3004 Test Method for Evaluation of Seal Quality and Integrity Using Airborne Ultrasound

    F3039 Test Method for Detecting Leaks in Nonporous Packaging or Flexible Barrier Materials by Dye Penetration

    EN/ISO Standards

    EN 868/1 Annex C Gurley, Schopper, Dye Penetration

    ISO 10993 Biological Evaluation of Medical Devices

    ISO 11607–1 Packaging for Terminally Sterilized Medical Devices, Annex C

    ISO 15105–1 Plastics--Film and Sheeting--Determination of Gas Transmission Rate--Part 1: Differential-Pressure Method

    ISO 15105–2 Plastics--Film and Sheeting--Determination of Gas Transmission Rate--Part 2: Equal-Pressure Method

    ISO 2556 Plastics--Determination of Gas Transmission Rate of Films and Thin Sheets Under Atmospheric Pressure--Manometric Method

    ISO 5636–5 Paper and Board--Determination of Air Permeance (Medium Range)--Part 5: Gurley Method

    Military Specification

    Mil Spec 36954C Bacterial Filtration Efficiency

    TAPPI Standards

    TAPPI T 404 Tensile Breaking Strength and Elongation of Paper and Paperboard

    TAPPI T 460 Air Resistance of Paper (Gurley Method)

    TAPPI T 494 Tensile Breaking Properties of Paper and Paperboard (Using Constant Rate of Elongation Apparatus)

    TAPPI T 536 Resistance of Paper to Passage of Air (High Pressure Gurley Method)

    TAPPI T 547 Air Permeance of Paper and Paperboard (Sheffield Method)

    ICS Code

    ICS Number Code 11.020 (Medical sciences and health care facilities in general); 55.020 (Packaging and distibution of goods in general)

    UNSPSC Code

    UNSPSC Code 24120000(Packaging materials)

    Referencing This Standard

    DOI: 10.1520/F2097-14

    ASTM International is a member of CrossRef.

    Citation Format

    ASTM F2097-14, Standard Guide for Design and Evaluation of Primary Flexible Packaging for Medical Products, ASTM International, West Conshohocken, PA, 2014,

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