The main task of technical committees is to prepare International Standards. Draft International Standards adopted by the technical committees are circulated to. à aiguille interne. STANDARD. ISO. Second edition. Reference number. ISO (E). Provläsningsexemplar / Preview. STANDARD. ISO. Second edition. Reference number. ISO (E). This is a free 4 page sample. Access the full version online.
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Part 1 General requirements do The technical committee has reviewed the 10555–5 of the following International Standard referred in this adopted standard and has decided that it is acceptable for use in conjunction with this standard: Certain conventions are, however, not identical to those used in Indian Standards.
The details of conditions under which the licence for the use 15055-5 the Standard Mark may be granted to manufacturers or producers may be obtained from the Bureau of Indian Standards. Attention is particularly drawn to the following: This does not preclude the free use, in the course of implementing the standard, of necessary details, such as symbols and sizes, type or grade designations. Rigid tube with one end sharpened to facilitate entry into body tissue.
Designation and catalogue 10555–5 CCR colours.
Round the calculated average water fiowrate to the nearest whole number of millilitres. All standards are subject to revision, and parties to agreements based on this part of ISO are encouraged to investigate the possibility of applying the most recent editions of the standards indicated below.
Suggested colour references for opaque naaterials are given in annex C. Measure the time taken for fluid to form the first falling drop at the back of the vent fitting. Add the following reference: I Principle A force is applied successively tensile and connpress- ive to the needle tube and needle hub and the tube- hub union is then examined for loosening. The catheter tube may have a single lumen iiso multiple lumens. Annex D shows examples of typical needle point geom- etries.
EN ISO – European Standards
Blood flow into ieo needle hub. This Indian Standard has been developed from Doc No.: The corresponding Indian Standards which are to be substituted in their places are listed below along with their degree of equivalence for the editions indicated: Pages 1 and 2 4.
In this adopted standard, reference appears to certain International Standards for which Indian Standards also exist. Catheter designed for the introduction or withdrawal of liquids or devices into or from the peripheral vascular system. Figure 1 — Typical over-needle peripheral intravascular catheter NOTE 2 At 1055-5 time of publication of this part of ISOthere is no acceptable, validated test method to determine radio-detectability.
Page 3, subclause 4.
Review of Indian Standards Amendments are issued to standards as the need arises on the basis of comments.
International Standard ISO An example of a suitable apparatus is shown in fig- ure B. For the purpose of deciding whether a particular requirement of this standard is complied with, the final value, observed or calculated expressing the result of a test or analysis, shall be rounded off in accordance with IS 2: The assembly comprising at least a needle tube attached to and communicating with a needle hub.
Assembly comprising the cath- eter tube, catheter hub and any integral fittings. Assembly comprising at least a needle tube attached to, ixo communicating with, a needle hub. Until that time, a manufacturer may label his product “radio- opaque” provided he can support this claim 10555-5 demonstrat- ing that he has an appropriate method for showing radio- opacity. When tested in accordance with annex E, fluid shall not leak out of the vent fitting within 15 s. Bureau of Indian Standards BIS is a statutory institution established under the Bureau of Indian Standards Act, to promote harmonious development of the activities of standardization, marking and quality certification of goods and attending to connected matters in the country.
Search the history of over billion web pages on the Internet. Users of Indian Standards should ascertain that they are in possession of the 105555-5 amendments or edition by referring to the latest issue of ‘BIS Catalogue’ and ‘Standards: If a steel tube is used, it shall connply with ISO Limited collection of colours.
NOTE To improve the visibility of the solution, a colorant such as red or blue food dye may be incorporated. Other parts of this standard are as follows: NOTE 3 The point should be designed to be noncoring. Details of which is given in 10555- Annex A.
Available from 1055-5 Color, N. Fixed or removable fitting per- mitting venting of air while restricting or preferably preventing the escape of blood. I Principle Water is allowed to flow through the catheter and the amount of flow is measured either volumetrically or gravimetrically. Fitting attached to the needle tube, providing communication with its bore.
At the time of publication, the editions indicated were valid. E-5 Test report The test report shall contain at least the following information: No part of the these publications may be lso in any form without the prior permission in writing of BIS. Standards are also reviewed periodically; a standard alongwith amendments is reaffirmed when such review indicates that no changes 01555-5 needed; if the review indicates that changes are needed, it is taken up for revision.
Intravascular catheters ISO , -3, -4, -5
The number of significant places retained in the rounded off value should be the same as that of the specified value in this standard. An approved test method for producing a value of radio-detectability will be established. The fluid pathway in the needle shall be free of unintended obstructions that would prevent flashback. The fluid is allowed to flow into the needle, and the time taken for fluid to leak through the vent fitting is measured.
When the needle is fully inserted into the catheter unit, the catheter tube shall neither extend beyond the heel of the needle bevel nor be nnore than 1 nnnn fronn it see dinnension a in figure 1.
Peripheral intravascular catheter designed for the introduction of withdrawal of liquids or devices into or from the peripheral vascular system.