ASTM E1093-91(2019)
(Specification)Standard Specification for Glass Prothrombin Pipet, Disposable
Standard Specification for Glass Prothrombin Pipet, Disposable
ABSTRACT
This specification covers the physical requirements and corresponding test methods for disposable glass Prothrombin pipets suitable for use in micro techniques for estimating Prothrombin time. The pipet shall be made of Type 1, Class B borosilicate glass, or Type 2 soda lime glass. The physical properties to which the pipets should adhere to are those for design, dimensions, capacity (accuracy and coefficient of variation), graduation lines, pipet nomenclature, blow-out delivery, color coding, marking permanency, and lot control.
SCOPE
1.1 This specification covers a glass disposable Prothrombin pipet suitable for use in micro techniques for estimation of Prothrombin time.
1.2 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.
1.3 This precautionary statement pertains only to the test method portion, Section 8, of this specification. 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, health, and environmental practices and determine the applicability of regulatory limitations prior to use.
1.4 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.
General Information
- Status
- Published
- Publication Date
- 31-Dec-2018
- Technical Committee
- E41 - Laboratory Apparatus
- Drafting Committee
- E41.01 - Laboratory Ware and Supplies
Relations
- Effective Date
- 01-Jan-2019
- Effective Date
- 01-Feb-2024
- Effective Date
- 01-Jan-2018
- Effective Date
- 01-Dec-2011
- Effective Date
- 01-Nov-2006
- Effective Date
- 15-Aug-1993
- Effective Date
- 15-Aug-1993
Overview
ASTM E1093-91(2019) is the internationally recognized standard specification for disposable glass Prothrombin pipets, suited for micro techniques to estimate Prothrombin time in laboratory settings. Developed by ASTM International, this standard defines the physical requirements and test methods for these pipets, ensuring quality, safety, and accuracy in coagulation testing. The specification supports laboratories and manufacturers in delivering reliable single-use pipets made from either Type 1, Class B borosilicate glass or Type 2 soda lime glass, following stringent design and performance criteria.
Key Topics
- Materials: The standard requires pipets to be manufactured from specified glass types, ensuring chemical resistance and structural integrity.
- Design and Dimensions: Pipets must be one-piece, straight, and uniform in bore, adhering to dimensional tolerances for consistent performance.
- Capacity and Accuracy: Each pipet is calibrated to "to deliver" (T.D.) specified volumes, with accuracy and coefficient of variation tightly controlled.
- Graduation and Markings: Clear, permanent calibration lines at 0.1 mL and 0.2 mL ensure accurate measurement, aided by distinct color coding as per ISO 1769.
- Blow-Out Delivery: Specific delivery methods are outlined, requiring full evacuation of contents as part of proper laboratory technique.
- Marking Permanency: Markings must endure a standard permanency test to remain legible through routine handling and one-time use.
- Lot Control: Pipet packaging must carry lot or control numbers for traceability to raw materials and manufacturing batches.
Applications
Disposable glass Prothrombin pipets compliant with ASTM E1093-91(2019) are essential in:
- Clinical Laboratories: Used in coagulation testing, particularly for estimating Prothrombin time, supporting the diagnosis and monitoring of coagulation disorders.
- Medical Research: Ensures accuracy in small-volume sample delivery for micro techniques, essential for reliable research results.
- Manufacturing Quality Assurance: Laboratories engaged in pipet production use this standard to validate manufacturing processes and batch quality.
- Regulatory Compliance: Institutions requiring adherence to international standards rely on this specification for best practices in laboratory glassware usage.
By adhering to this specification, users are assured of high-precision, single-use pipets engineered for accuracy, safety, and traceability-critical factors in any clinical or research environment. Proper training and reference to regulatory guidelines are advised to address all safety and health concerns related to glassware use.
Related Standards
- ASTM E438 – Specification for Glasses in Laboratory Apparatus: Defines material requirements for glass used in laboratories.
- ISO 1769 – Laboratory Glassware: Pipettes, Color Coding: Specifies international standards for color coding capacities on laboratory pipettes.
Summary
ASTM E1093-91(2019) standardizes the design, manufacture, and testing of disposable glass Prothrombin pipets, facilitating precision and consistency in coagulation testing worldwide. This specification supports best practices in laboratory glassware, ensuring that healthcare and scientific professionals have access to dependable and standardized pipetting tools for critical micro techniques. For full compliance and operational excellence, laboratories and manufacturers should adopt ASTM E1093-91(2019) as their reference for single-use Prothrombin pipets.
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Frequently Asked Questions
ASTM E1093-91(2019) is a technical specification published by ASTM International. Its full title is "Standard Specification for Glass Prothrombin Pipet, Disposable". This standard covers: ABSTRACT This specification covers the physical requirements and corresponding test methods for disposable glass Prothrombin pipets suitable for use in micro techniques for estimating Prothrombin time. The pipet shall be made of Type 1, Class B borosilicate glass, or Type 2 soda lime glass. The physical properties to which the pipets should adhere to are those for design, dimensions, capacity (accuracy and coefficient of variation), graduation lines, pipet nomenclature, blow-out delivery, color coding, marking permanency, and lot control. SCOPE 1.1 This specification covers a glass disposable Prothrombin pipet suitable for use in micro techniques for estimation of Prothrombin time. 1.2 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard. 1.3 This precautionary statement pertains only to the test method portion, Section 8, of this specification. 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, health, and environmental practices and determine the applicability of regulatory limitations prior to use. 1.4 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.
ABSTRACT This specification covers the physical requirements and corresponding test methods for disposable glass Prothrombin pipets suitable for use in micro techniques for estimating Prothrombin time. The pipet shall be made of Type 1, Class B borosilicate glass, or Type 2 soda lime glass. The physical properties to which the pipets should adhere to are those for design, dimensions, capacity (accuracy and coefficient of variation), graduation lines, pipet nomenclature, blow-out delivery, color coding, marking permanency, and lot control. SCOPE 1.1 This specification covers a glass disposable Prothrombin pipet suitable for use in micro techniques for estimation of Prothrombin time. 1.2 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard. 1.3 This precautionary statement pertains only to the test method portion, Section 8, of this specification. 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, health, and environmental practices and determine the applicability of regulatory limitations prior to use. 1.4 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.
ASTM E1093-91(2019) is classified under the following ICS (International Classification for Standards) categories: 11.100.99 - Other standards related to laboratory medicine. The ICS classification helps identify the subject area and facilitates finding related standards.
ASTM E1093-91(2019) has the following relationships with other standards: It is inter standard links to ASTM E1093-91(2012), ASTM E438-92(2024), ASTM E438-92(2018), ASTM E438-92(2011), ASTM E438-92(2006), ASTM E438-92(1996), ASTM E438-92(2001)e1. Understanding these relationships helps ensure you are using the most current and applicable version of the standard.
ASTM E1093-91(2019) 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: E1093 −91 (Reapproved 2019)
Standard Specification for
Glass Prothrombin Pipet, Disposable
This standard is issued under the fixed designation E1093; the number immediately following the designation indicates the year of
original adoption or, in the case of revision, the year of last revision. A number in parentheses indicates the year of last reapproval. A
superscript epsilon (´) indicates an editorial change since the last revision or reapproval.
1. Scope 3.1.2 coeffıcient of variation—the expected distribution of
individual volumes around the mean volume.
1.1 ThisspecificationcoversaglassdisposableProthrombin
3.1.3 disposable—Prothrombin pipets which are intended to
pipet suitable for use in micro techniques for estimation of
be used once only and then discarded.
Prothrombin time.
1.2 The values stated in SI units are to be regarded as NOTE 1—Such pipets will only be expected to provide their specified
performance during the original operation.
standard. No other units of measurement are included in this
standard.
4. Classification
1.3 This precautionary statement pertains only to the test
4.1 This specification covers only one glass pipet as illus-
method portion, Section 8, of this specification. This standard
trated in Fig. X1.1.
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
5. Materials and Manufacture
standard to establish appropriate safety, health, and environ-
5.1 The pipet shall be made of borosilicate glass, Type 1;
mental practices and determine the applicability of regulatory
Class B, or soda lime glass, Type 2, in accordance with
limitations prior to use.
Specification E438.
1.4 This international standard was developed in accor-
dance with internationally recognized principles on standard-
6. Physical Properties
ization established in the Decision on Principles for the
Development of International Standards, Guides and Recom- 6.1 Design—The Prothrombin pipet shall be made of one
piececonstructionglasstubingthatisstraightandwithuniform
mendations issued by the World Trade Organization Technical
Barriers to Trade (TBT) Committee. bore and lightly firepolished on both ends. The pipet shall be
made to the dimensions as specified in Fig. X1.1.
2. Referenced Documents
6.2 Dimensions—The pipet shall be made of tubing with a
2.1 ASTM Standards:
minimum outside diameter (o.d.) of 2.3 mm with an inside
E438 Specification for Glasses in Laboratory Apparatus
diameter (i.d.) of 1.7 mm. The uniformity of the bore shall be
2.2 ISO Standard:
60.05 mm throughout the straight portion of the pipet. The
1769 Laboratory Glassware—Pipettes—Color Coding
pipet shall be a minimum of 160 mm long.
6.3 Capacity—The pipet shall be calibrated “to deliver”
3. Terminology
(T.D.) 0.1 and 0.2 mL at 20 °C. Marking shall be as specified
3.1 Definitions of Terms Specific to This Standard:
in 6.5.
3.1.1 accuracy—the expected distribution of mean volumes
6.3.1 Accuracy (see 3.1.1)—The accuracy from stated vol-
around the stated volume.
ume shall be 62.0 % for the 0.1 and 0.2-mLcapacity and shall
be determined as specified in 8.1.
6.3.2 Coeffıcient of Variation (see 3.1.2)—The coefficient of
This specification is under the jurisdiction of ASTM Committee E41 on
variation from stated volume for the 0.1 and 0.2-mL capacity
Laboratory Apparatus and is the direct responsibility of Subcommittee E41.01 on
Laboratory Ware and Supplies.
shall not exceed 2.0 % and shall be determined as specified in
Current edition approved Jan. 1, 2019. Published January 2019. Originally
8.1.
approved in 1986. Last previous edition approved in 2012 as E1093 – 91(2012).
DOI: 10.1520/E1093-91R19.
6.4 Graduation Lines—The pipet shall be calibrated and
For referenced ASTM standards, visit the ASTM website, www.astm.org, or
marked with graduation lines at 0.1 and 0.2 mLfrom the tip of
contact ASTM Customer Service at service@astm.org. For Annual Book of ASTM
the pipet.The graduation lines shall be 0.3 6 0.1 mm and shall
Standards volume information, refer to the standard’s Document Summary page on
the ASTM website. completely encircle the tube.
Available from International Organization for Standardization (ISO), ISO
6.5 Pipet Nomenclature—The pipet shall be marked with
Central Secretariat, BIBC II, Chemin de Blandonnet 8, CP 401, 1214 Vernier,
Geneva, Switzerland, http://www.iso.org. 0.1 and 0.2-mL markings slightly above the graduation lines.
Copyright © ASTM International, 100 Barr Harbor Drive, PO Box C700, West Conshohocken, PA 19428-2959. United States
E1093 − 91 (2019)
The pipet may be marked with the inscription T.D. 20 °C, or 8.2 Calculation—Calculate the volume, V, of a micropipet
the manufacturer’s or vendor’s name or trademark, or both. from the weighings, in air, as follows:
6.6 Blow-out Delivery—The Prothrombin pipet is designed V 5 W 3Z (1)
as a dual delivery system for the determinations of coagulation
where:
assays.Whenutilizingthe0.2mLcalibrationline,thetipofthe
W = apparent mass of liquid (water), weighed in air, and
pipet should contact the wall of the receiving vessel and allow
Z = apparent specific volume of liquid (water).
the pipet to drain freely. The remaining quantity of liquid is to
Values of Z for water are given in the appendix.
be blown out into the center of the receiving vessel. When
utilizing the 0.1 mL calibration line the contents are t
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