Standard Classification for Vinyl Chloride Plastics Used in Biomedical Application

SIGNIFICANCE AND USE
4.1 This classification was developed to permit the addition of descriptive symbols and values for further new formulations with improved properties without complete reorganization of the standard and to facilitate the incorporation of future new test methods to keep pace with changing industry requirements.
SCOPE
1.1 This classification provides guidance to engineers and users in the selection of practical vinyl chloride plastics for medical applications and further provides a method for specifying these materials by use of a simple line call-out designation. This classification excludes vinyl chloride plastics used in long-term implants.  
1.2 Use is made of a classification scheme based on the premise that the composition of vinyl chloride plastics, copolymers, fillers, plasticizers, stabilizers, and other additives in these systems can be arranged into characteristic material designations.  
1.3 In all cases where the provisions of this classification system would conflict with those of the detailed specification for a particular device, the latter shall take precedence.
Note 1: For cases in which the vinyl chloride plastic may be used for purposes where the requirements are too specific to be completely described by this classification system, it is advisable for the purchaser to consult the supplier to secure adjustment of the properties to suit the actual conditions to which the device is to be subjected.  
1.4 The biocompatibility of vinyl chloride plastics as a class of materials has not been established. Since many compositions and formulations fall under this class, it is essential that the fabricators/device manufacturers assure the safety and efficacy of the specific composition or formulation, in its intended application, using state-of-the-art test methods.  
1.5 This classification is to assist the interface between the material supplier and the device manufacturer (fabricator) who purchases a formulated vinyl chloride plastic for a component. For those device manufacturers (fabricators) who do their own formulating, compounding, extrusion, molding, and so forth, this classification does not apply.  
1.6 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety and health practices and determine the applicability of regulatory limitations prior to use.

General Information

Status
Published
Publication Date
28-Feb-2015
Drafting Committee
F04.11 - Polymeric Materials

Relations

Effective Date
01-Mar-2015
Effective Date
01-Jan-2020
Effective Date
01-Apr-2016
Effective Date
01-Feb-2011
Effective Date
01-Jun-2010
Effective Date
01-Jan-2009
Effective Date
15-Jun-2008
Effective Date
15-May-2007
Effective Date
01-Dec-2006
Effective Date
01-Apr-2006
Effective Date
01-Nov-2005
Effective Date
01-Sep-2005
Effective Date
01-Jul-2004
Effective Date
01-May-2004
Effective Date
01-Mar-2004

Overview

ASTM F665-09(2015): Standard Classification for Vinyl Chloride Plastics Used in Biomedical Application provides a systematic approach for classifying vinyl chloride plastics (such as polyvinyl chloride, PVC) intended for use in medical and biomedical devices, while excluding materials used in long-term implants. This standard, developed by ASTM International, aims to guide engineers, medical device manufacturers, and material suppliers in the selection and specification of vinyl chloride plastics for biomedical applications.

A key advantage of this classification system is its flexibility - it allows for the addition of new formulations and properties, and can incorporate future test methods in line with evolving industry requirements.

Key Topics

1. Material Composition and Classification

  • The standard uses a descriptive letter and number system to denote the presence and type of additives such as copolymers, plasticizers, stabilizers, fillers, colorants, and lubricants.
  • Only poly(vinyl chloride) is classified as a homopolymer within this standard; copolymers are also clearly categorized.
  • The classification excludes vinyl chloride plastics for long-term implant applications.

2. Specification Methodology

  • Utilizes a simple line call-out designation for specifying material formulations.
  • Supports clear communication between material suppliers and device manufacturers when purchasing formulated vinyl chloride plastics.

3. Physical Properties and Testing

  • Key physical properties such as hardness (Shore A), tensile strength, and elongation are incorporated in the classification numbers.
  • Standard test methods referenced include ASTM D2240 (Durometer Hardness), D882 (Tensile Properties), D792 (Density), D570 (Water Absorption), among others.

4. Biocompatibility Considerations

  • The biocompatibility of vinyl chloride plastics as a class has not been established; testing is required for each specific composition and application.
  • Recommends biological evaluation following guidelines such as ISO 10993 and ASTM F748 for medical devices.

5. Safety and Compliance

  • Users must determine relevant safety, health practices, and regulatory limitations before adopting classified materials in medical device manufacturing.

Applications

The ASTM F665-09(2015) standard is widely applied in the development and selection of vinyl chloride plastics for biomedical and healthcare devices (excluding long-term implants), including:

  • Tubing, connectors, and containers for temporary medical use
  • Catheters, blood bags, and transfusion sets
  • Medical device housings and disposable instruments
  • Packaging materials for pharmaceutical products

It ensures a consistent, transparent method for specifying materials, facilitating efficient communication between suppliers and medical device manufacturers, and supporting regulatory compliance by using established properties and test methods.

Related Standards

  • ASTM D2240: Test Method for Rubber Property-Durometer Hardness
  • ASTM D882: Test Method for Tensile Properties of Thin Plastic Sheeting
  • ASTM D570: Test Method for Water Absorption of Plastics
  • ASTM D792: Test Methods for Density and Specific Gravity of Plastics
  • ASTM F748: Practice for Selecting Generic Biological Test Methods for Materials and Devices
  • ISO 10993: Biological Evaluation of Medical Devices
  • 21 CFR (Code of Federal Regulations): Food and Drug Administration regulations on medical device materials

Practical Value

Adopting ASTM F665-09(2015) streamlines the process of material selection for biomedical applications by providing a comprehensive classification system. It supports safer medical device development through established reference methods for chemical, mechanical, and biological property evaluation. Ultimately, this standard enhances efficiency, traceability, and regulatory alignment for manufacturers, material suppliers, and end users in the healthcare sector-all while keeping pace with ongoing advancements in polymer materials technology.

Keywords: ASTM F665, vinyl chloride plastics, biomedical application, medical device materials, PVC classification, material specification, biocompatibility, ASTM standards, healthcare polymers.

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Frequently Asked Questions

ASTM F665-09(2015) is a standard published by ASTM International. Its full title is "Standard Classification for Vinyl Chloride Plastics Used in Biomedical Application". This standard covers: SIGNIFICANCE AND USE 4.1 This classification was developed to permit the addition of descriptive symbols and values for further new formulations with improved properties without complete reorganization of the standard and to facilitate the incorporation of future new test methods to keep pace with changing industry requirements. SCOPE 1.1 This classification provides guidance to engineers and users in the selection of practical vinyl chloride plastics for medical applications and further provides a method for specifying these materials by use of a simple line call-out designation. This classification excludes vinyl chloride plastics used in long-term implants. 1.2 Use is made of a classification scheme based on the premise that the composition of vinyl chloride plastics, copolymers, fillers, plasticizers, stabilizers, and other additives in these systems can be arranged into characteristic material designations. 1.3 In all cases where the provisions of this classification system would conflict with those of the detailed specification for a particular device, the latter shall take precedence. Note 1: For cases in which the vinyl chloride plastic may be used for purposes where the requirements are too specific to be completely described by this classification system, it is advisable for the purchaser to consult the supplier to secure adjustment of the properties to suit the actual conditions to which the device is to be subjected. 1.4 The biocompatibility of vinyl chloride plastics as a class of materials has not been established. Since many compositions and formulations fall under this class, it is essential that the fabricators/device manufacturers assure the safety and efficacy of the specific composition or formulation, in its intended application, using state-of-the-art test methods. 1.5 This classification is to assist the interface between the material supplier and the device manufacturer (fabricator) who purchases a formulated vinyl chloride plastic for a component. For those device manufacturers (fabricators) who do their own formulating, compounding, extrusion, molding, and so forth, this classification does not apply. 1.6 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety and health practices and determine the applicability of regulatory limitations prior to use.

SIGNIFICANCE AND USE 4.1 This classification was developed to permit the addition of descriptive symbols and values for further new formulations with improved properties without complete reorganization of the standard and to facilitate the incorporation of future new test methods to keep pace with changing industry requirements. SCOPE 1.1 This classification provides guidance to engineers and users in the selection of practical vinyl chloride plastics for medical applications and further provides a method for specifying these materials by use of a simple line call-out designation. This classification excludes vinyl chloride plastics used in long-term implants. 1.2 Use is made of a classification scheme based on the premise that the composition of vinyl chloride plastics, copolymers, fillers, plasticizers, stabilizers, and other additives in these systems can be arranged into characteristic material designations. 1.3 In all cases where the provisions of this classification system would conflict with those of the detailed specification for a particular device, the latter shall take precedence. Note 1: For cases in which the vinyl chloride plastic may be used for purposes where the requirements are too specific to be completely described by this classification system, it is advisable for the purchaser to consult the supplier to secure adjustment of the properties to suit the actual conditions to which the device is to be subjected. 1.4 The biocompatibility of vinyl chloride plastics as a class of materials has not been established. Since many compositions and formulations fall under this class, it is essential that the fabricators/device manufacturers assure the safety and efficacy of the specific composition or formulation, in its intended application, using state-of-the-art test methods. 1.5 This classification is to assist the interface between the material supplier and the device manufacturer (fabricator) who purchases a formulated vinyl chloride plastic for a component. For those device manufacturers (fabricators) who do their own formulating, compounding, extrusion, molding, and so forth, this classification does not apply. 1.6 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety and health practices and determine the applicability of regulatory limitations prior to use.

ASTM F665-09(2015) is classified under the following ICS (International Classification for Standards) categories: 07.100.10 - Medical microbiology; 11.040.40 - Implants for surgery, prosthetics and orthotics. The ICS classification helps identify the subject area and facilitates finding related standards.

ASTM F665-09(2015) has the following relationships with other standards: It is inter standard links to ASTM F665-09, ASTM D149-20, ASTM F748-16, ASTM D2124-99(2011), ASTM F748-06(2010), ASTM D882-09, ASTM D792-08, ASTM D257-07, ASTM F748-06, ASTM D543-06, ASTM D570-98(2005), ASTM D257-99(2005), ASTM D2124-99(2004), ASTM F748-04, ASTM D150-98(2004). Understanding these relationships helps ensure you are using the most current and applicable version of the standard.

ASTM F665-09(2015) is available in PDF format for immediate download after purchase. The document can be added to your cart and obtained through the secure checkout process. Digital delivery ensures instant access to the complete standard document.

Standards Content (Sample)


This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the
Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.
Designation:F665 −09 (Reapproved 2015)
Standard Classification for
Vinyl Chloride Plastics Used in Biomedical Application
ThisstandardisissuedunderthefixeddesignationF665;thenumberimmediatelyfollowingthedesignationindicatestheyearoforiginal
adoption or, in the case of revision, the year of last revision.Anumber in parentheses indicates the year of last reapproval.Asuperscript
epsilon (´) indicates an editorial change since the last revision or reapproval.
1. Scope 2. Referenced Documents
1.1 This classification provides guidance to engineers and 2.1 ASTM Standards:
users in the selection of practical vinyl chloride plastics for D149 Test Method for Dielectric Breakdown Voltage and
medical applications and further provides a method for speci- DielectricStrengthofSolidElectricalInsulatingMaterials
fying these materials by use of a simple line call-out designa- at Commercial Power Frequencies
tion.This classification excludes vinyl chloride plastics used in D150 Test Methods forAC Loss Characteristics and Permit-
long-term implants. tivity (Dielectric Constant) of Solid Electrical Insulation
D257 Test Methods for DC Resistance or Conductance of
1.2 Use is made of a classification scheme based on the
Insulating Materials
premise that the composition of vinyl chloride plastics,
D543 Practices for Evaluating the Resistance of Plastics to
copolymers, fillers, plasticizers, stabilizers, and other additives
Chemical Reagents
in these systems can be arranged into characteristic material
D570 Test Method for Water Absorption of Plastics
designations.
D792 Test Methods for Density and Specific Gravity (Rela-
1.3 In all cases where the provisions of this classification
tive Density) of Plastics by Displacement
system would conflict with those of the detailed specification
D882 Test Method for Tensile Properties of Thin Plastic
for a particular device, the latter shall take precedence.
Sheeting
NOTE 1—For cases in which the vinyl chloride plastic may be used for
D955 Test Method of Measuring Shrinkage from Mold
purposes where the requirements are too specific to be completely
Dimensions of Thermoplastics
described by this classification system, it is advisable for the purchaser to
D2124 Test Method forAnalysis of Components in Poly(Vi-
consultthesuppliertosecureadjustmentofthepropertiestosuittheactual
conditions to which the device is to be subjected.
nyl Chloride) Compounds Using an Infrared Spectropho-
tometric Technique
1.4 The biocompatibility of vinyl chloride plastics as a class
D2240 Test Method for Rubber Property—Durometer Hard-
of materials has not been established. Since many composi-
ness
tions and formulations fall under this class, it is essential that
F748 PracticeforSelectingGenericBiologicalTestMethods
the fabricators/device manufacturers assure the safety and
for Materials and Devices
efficacy of the specific composition or formulation, in its
F1251 Terminology Relating to Polymeric Biomaterials in
intended application, using state-of-the-art test methods.
Medical and Surgical Devices (Withdrawn 2012)
1.5 This classification is to assist the interface between the
2.2 Other Standards:
material supplier and the device manufacturer (fabricator) who
21 CFR Code of Federal Regulations
purchases a formulated vinyl chloride plastic for a component.
2.3 ISO Standard:
For those device manufacturers (fabricators) who do their own
ISO 10993 Biological Evaluation of Medical Devices
formulating, compounding, extrusion, molding, and so forth,
this classification does not apply.
3. Terminology
1.6 This standard does not purport to address all of the
3.1 Definitions:
safety concerns, if any, associated with its use. It is the
responsibility of the user of this standard to establish appro-
priate safety and health practices and determine the applica-
For referenced ASTM standards, visit the ASTM website, www.astm.org, or
contact ASTM Customer Service at service@astm.org. For Annual Book of ASTM
bility of regulatory limitations prior to use.
Standards volume information, refer to the standard’s Document Summary page on
the ASTM website.
1 3
This classification is under the jurisdiction of ASTM Committee F04 on The last approved version of this historical standard is referenced on
Medical and Surgical Materials and Devicesand is the direct responsibility of www.astm.org.
Subcommittee F04.11 on Polymeric Materials. Available from Superintendent of Documents, U.S. Government Printing
Current edition approved March 1, 2015. Published May 2015. Originally Office, Washington, DC 20402.
approved in 1980. Last previous edition approved in 2009 as F665 – 09. DOI: Available fromAmerican National Standards Institute (ANSI), 25 W. 43rd St.,
10.1520/F0665-09R15. 4th Floor, New York, NY 10036, http://www.ansi.org.
Copyright © ASTM International, 100 Barr Harbor Drive, PO Box C700, West Conshohocken, PA 19428-2959. United States
F665−09 (2015)
3.1.1 filler—a relatively inert material added to a plastic to
Letter Designation Secondary Plasticizer
modify its strength, permanence, working properties, or other
A none
qualities, or to lower costs.
B alkyl epoxy stearates
C epoxidized tall oil
3.1.2 plasticizer—a substance incorporated into a material
D epoxidized soybean oil
to increase its workability, flexibility, or distensibility.
E epoxidized linseed oil
F epoxidized sunflower oil
3.1.3 stabilizer—a substance added to a plastic that will
Z other
retard the deterioration of the plastic due to the effects of heat,
light, or oxidation.
Number Primary Plasticizer
3.1.4 vinyl chloride plastics—plastics based on polymers of
1 none
vinyl chloride or copolymers of vinyl chloride with other
2 adipic acid derivatives
monomers, the vinyl chloride being the comonomer of the 3 azelaic acid derivatives
4 benzoic acid derivatives
highest concentration by mass.
5 citric acid derivatives
6 isophthalic acid derivatives
3.2 See Terminology F1251 for additional terms relevant to
7 myristic acid derivatives
polymers.
8 phosphoric acid derivatives
9 phthalic acid derivatives
10 sebacic acid derivatives
4. Significance and Use
11 terephthalic acid derivatives
4.1 This classification was developed to permit the addition
12 polyethers
13 polyethylene glycols
of descriptive symbols and values for further new formulations
14 polyesters
with improved properties without complete reorganization of
999 other
the standard and to facilitate the incorporation of future new
5.5 Stabilizers—Stabilization systems are usually composed
test methods to keep pace with changing industry require-
of metal soap acceptors and auxiliary organic stabilizers. The
ments.
metal soap acceptors are characterized by the metal(s) present.
The following is a representative list of stabilizers. The
5. Formulation Designation
designation is obtained by using the prefix (C) followed by the
NOTE 2—No judgment is made by ASTM as to the suitability of
possible compounds classified by the following system to any specific
letter for the metal, followed by the number for the chelator
biomedical use. Knowledge of formulation composition will only aid in
used. In the event that more than one in each category is
evaluation of a composition for suitability.
present, separate multiple letter or number designations, or
5.1 A letter/number system that will give guidance to the
both, by a comma.
engineer/user as to the nature of the formulation shall be used.
Letter Metal in Soap Acceptor
A general knowledge of the types of additives employed will
A none
aid in the evaluation of a particular formulation’s utility in a
B barium
medical application.
C calcium
D cadmium
5.2 Homopolymer—Bydefinition,onlyonehomopolymeris
E magnesium
covered by this classification: poly(vinyl chloride).
F lead
G strontium
5.3 Copolymer—The following is a representative list of
H
...

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