Standard Specification for Blood Sedimentation Tube, Wintrobe, Glass, Disposable

ABSTRACT
This specification covers disposable blood sedimentation tubes suitable for determining sedimentation rates and the volume of packed red blood cells. This specification covers a tube intended for one-time use only. The tubes shall be fabricated borosilicate glass, Type I, Class B, or from soda lime glass, Type II. The tubes shall be tested for their marking permanency and resistance to centrifugal test.
SCOPE
1.1 This specification covers disposable blood sedimentation tubes suitable for determining sedimentation rates and the volume of packed red blood cells.  
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 The following precautionary statement pertains only to the test method portion, Section 7 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 and health practices and determine the applicability of regulatory limitations prior to use.

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NOTICE: This standard has either been superseded and replaced by a new version or withdrawn.
Contact ASTM International (www.astm.org) for the latest information
Designation:E1047 −85 (Reapproved 2015)
Standard Specification for
Blood Sedimentation Tube, Wintrobe, Glass, Disposable
This standard is issued under the fixed designation E1047; the number immediately following the designation indicates the year of
original adoption or, in the case of revision, the year of last revision.Anumber in parentheses indicates the year of last reapproval.A
superscript epsilon (´) indicates an editorial change since the last revision or reapproval.
1. Scope 4. Classification
4.1 This specification covers a tube that is intended to be
1.1 This specification covers disposable blood sedimenta-
usedonetimeonly.Itisnottobeconfusedwithareusabletube
tion tubes suitable for determining sedimentation rates and the
that is described in other published standards.
volume of packed red blood cells.
1.2 The values stated in SI units are to be regarded as
5. Materials
standard. No other units of measurement are included in this
5.1 Glass—The tubes made to this specification shall be
standard.
fabricatedborosilicateglass,TypeI,ClassB,orfromsodalime
1.3 The following precautionary statement pertains only to glass, Type II, in accordance with Specification E438.
the test method portion, Section 7 of this specification. This
6. Physical Requirements
standard does not purport to address all of the safety concerns,
if any, associated with its use. It is the responsibility of the user
6.1 Design—The tube shall be made of tubing with a
of this standard to establish appropriate safety and health
minimum wall thickness of 0.6 mm. The tube shall have a
practices and determine the applicability of regulatory limita-
cylindrical body terminating in a round bottom on the outside
tions prior to use.
and a flat bottom on the inside. The tube shall have a uniform
bore and a fire-polished top.
2. Referenced Documents
6.2 Workmanship—The tube shall be free as possible from
2.1 ASTM Standards:
visible defects which detract from its serviceability. The tube
E438Specification for Glasses in Laboratory Apparatus shall be well annealed so there will be no ring strain evident
when tested under a polariscope.
3. Terminology
6.3 Dimensions—The tube shall be made of tubing with an
3.1 Definitions of Terms Specific to This Standard: outside diameter (O.D.) of 5.0 6 0.5 mm and an inside
diameter (I.D.) of 2.9 to 3.5 mm. The uniformity of the bore
3.1.1 disposable, n—in accordance with this specification
shall be 60.15 mm throughout the tube. The tube shall be 110
and the expected product performance expressed in this
to 117 mm long and have a graduated scale of 100 mm.
standard, those tubes which are to be used one time only.Any
Manufacturers have the option to place additional graduation
institutionorindividualwhoreusesadisposabletubemustbear
lines on the tube to a maximum of 105 mm. Maximum overall
full responsibility for its safety and effectiveness.
tolerance on the total graduation scale shall be 61.0 mm. The
3.1.2 Wintrobe , n—surname of the individual responsible
tube shall be legibly marked with the maker’s or vendor’s
for the design of the reusableWintrobe tube and the method of
name or mark and possess a wide color band at the top of the
use for both reusable and disposable tubes.
tube for marking purposes.
6.4 Graduation Scale—The tube shall be graduated 100 to
105 6 1.0 mm in 1 mm divisions and numbered every
This specification is under the jurisdiction of ASTM Committee E41 on
centimetre with two sets of numerals. One set of graduation
Laboratory Apparatus and is the direct responsibility of Subcommittee E41.01 on
numerals shall be from 0 to 9 cm down the left side of the
Laboratory Ware and Supplies.
graduation scale and the other set of graduation numerals shall
CurrenteditionapprovedJune1,2015.PublishedJuly2015.Originallyapproved
in 1985. Last previous edition approved in 2010 as E1047–85(2010). DOI:
befrom1to10cm up the right side of the graduation scal
...


This document is not an ASTM standard and is intended only to provide the user of an ASTM standard an indication of what changes have been made to the previous version. Because
it may not be technically possible to adequately depict all changes accurately, ASTM recommends that users consult prior editions as appropriate. In all cases only the current version
of the standard as published by ASTM is to be considered the official document.
Designation: E1047 − 85 (Reapproved 2010) E1047 − 85 (Reapproved 2015)
Standard Specification for
Blood Sedimentation Tube, Wintrobe, Glass, Disposable
This standard is issued under the fixed designation E1047; 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
1.1 This specification covers disposable blood sedimentation tubes suitable for determining sedimentation rates and the volume
of packed red blood cells.
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 The following precautionary statement pertains only to the test method portion, Section 7 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 and health practices and determine the applicability of regulatory limitations prior to use.
2. Referenced Documents
2.1 ASTM Standards:
E438 Specification for Glasses in Laboratory Apparatus
3. Terminology
3.1 Definitions of Terms Specific to This Standard:
3.1.1 disposable, n—in accordance with this specification and the expected product performance expressed in this standard,
those tubes which are to be used one time only. Any institution or individual who reuses a disposable tube must bear full
responsibility for its safety and effectiveness.
3.1.2 Wintrobe , n—surname of the individual responsible for the design of the reusable Wintrobe tube and the method of use
for both reusable and disposable tubes.
4. Classification
4.1 This specification covers a tube that is intended to be used one time only. It is not to be confused with a reusable tube that
is described in other published standards.
5. Materials
5.1 Glass—The tubes made to this specification shall be fabricated borosilicate glass, Type I, Class B, or from soda lime glass,
Type II, in accordance with Specification E438.
6. Physical Requirements
6.1 Design—The tube shall be made of tubing with a minimum wall thickness of 0.6 mm. The tube shall have a cylindrical body
terminating in a round bottom on the outside and a flat bottom on the inside. The tube shall have a uniform bore and a fire-polished
top.
6.2 Workmanship—The tube shall be free as possible from visible defects which detract from its serviceability. The tube shall
be well annealed so there will be no ring strain evident when tested under a polariscope.
This specification is under the jurisdiction of ASTM Committee E41 on Laboratory Apparatus and is the direct responsibility of Subcommittee E41.01 on Laboratory
Ware and Supplies.
Current edition approved July 1, 2010June 1, 2015. Published July 2010July 2015. Originally approved in 1985. Last previous edition approved in 20052010 as E1047 – 85
(2005).(2010). DOI: 10.1520/E1047-85R10.10.1520/E1047-85R15.
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 Standards
volume information, refer to the standard’s Document Summary page on the ASTM website.
Wintrobe, M. M., “Laboratory Evaluation of Erythrocytes,” Clinical Hematology, Seventh E., 1974, pp. 109–134.
Copyright © ASTM International, 100 Barr Harbor Drive, PO Box C700, West Conshohocken, PA 19428-2959. United States
E1047 − 85 (2015)
6.3 Dimensions—The tube shall be made of tubing with an outside diameter (O.D.) of 5.0 6 0.5 mm and an inside diameter
(I.D.) of 2.9 to 3.5 mm. The uniformity of the bore shall be 60.15 mm throughout the tube. The
...

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