EN ISO 7886-1:1997
(Main)Sterile hypodermic syringes for single use - Part 1: Syringes for manual use (ISO 7886-1:1993, including Technical Corrigendum 1:1995)
Sterile hypodermic syringes for single use - Part 1: Syringes for manual use (ISO 7886-1:1993, including Technical Corrigendum 1:1995)
Specifies requirements (cleanliness, limits for acidity and alkalinity, limits for extractable metals, lubricant, tolerance on graduated capacity, graduated scale, barrel, piston/plunger assembly, nozzle, performance, packaging, labelling) for sterile single-use hypodermic syringes made of plastic materials and intended for the aspiration of fluids or for the injection of fluids immediately after filling. Excludes e.g. syringes for use with insulin, single-use syringes made of glass.
Sterile Einmalspritzen für medizinische Zwecke - Teil 1: Spritzen zum manuellen Gebrauch (ISO 7886-1:1993, einschließlich Technische Korrektur 1:1995)
Dieser Teil der ISO 7886 beschreibt die Anforderungen an sterile Einmalspritzen für medizinische Zwecke aus Kunststoffen für das Aufziehen von Flüssigkeiten oder die Injektion von Flüssigkeiten unmittelbar nach dem Füllen. Ausgenommen sind Insulin-Einmalspritzen nach ISO 8537, Einmalspritzen aus Glas, Spritzen mit fest verbundener Kanüle, Spritzen für Druckinfusionsapparate, vom Hersteller mit injizierbarer Zubereitung vorgefüllte Spritzen sowie Beilagespritzen, die vom Apotheker gefüllt werden.
Seringues hypodermiques stériles, non réutilisables - Partie 1: Seringues pour utilisation manuelle (ISO 7886-1:1993, Rectificatif Technique 1:1995 inclus)
La présente partie de l'ISO 7886 fixe les prescriptions relatives aux seringues hypodermiques stériles non réutilisables en matières plastiques, destinées à l'aspiration de liquides ou à l'injection de liquides immédiatement après leur remplissage. Elle n'est pas applicable aux seringues destinées à être utilisées avec de l'insuline (voir ISO 8537), aux seringues en verre non réutilisables, aux seringues avec aiguilles fixées de façon permanente, aux seringues pour pousse-seringues, aux seringues préremplies avec l'injection par le fabricant et aux seringues qui sont fournies avec l'injection sous forme de kit, destinées à être remplies par un pharmacien.
NOTE 1 Une deuxième partie de l'ISO 7886 est en préparation pour traiter des seringues pour pousse-seringues.
Sterilne podkožne injekcijske brizge za enkratno uporabo - 1. del: Injekcijske brizge za ročno injiciranje (ISO 7886-1:1993, vključno s tehničnim popravkom 1:1995)
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Standards Content (Sample)
2003-01.Slovenski inštitut za standardizacijo. Razmnoževanje celote ali delov tega standarda ni dovoljeno.Sterile Einmalspritzen für medizinische Zwecke - Teil 1: Spritzen zum manuellen Gebrauch (ISO 7886-1:1993, einschließlich Technische Korrektur 1:1995)Seringues hypodermiques stériles, non réutilisables - Partie 1: Seringues pour utilisation manuelle (ISO 7886-1:1993, Rectificatif Technique 1:1995 inclus)Sterile hypodermic syringes for single use - Part 1: Syringes for manual use (ISO 7886-1:1993, including Technical Corrigendum 1:1995)11.040.25Injekcijske brizge, igle in katetriSyringes, needles an cathetersICS:Ta slovenski standard je istoveten z:EN ISO 7886-1:1997SIST EN ISO 7886-1:2000en01-januar-2000SIST EN ISO 7886-1:2000SLOVENSKI
STANDARD
INTERNATIONAL STANDARD ISO 7886-1 First edition 1993-10-01 Sterile hypodermic syringes for Single use - Part 1: Syringes for manual use Seringues hypodermiques st&iles, non r&tilisables - Partie 1: Seringues pour utilisation manuelle Reference number ISO 7886-1: 1993(E) SIST EN ISO 7886-1:2000
ISO 7886=1:1993(E) Contents Page 1 Scope . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 2 Normative references . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 3 Definitions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .*. 1 4 Nomenclature . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .*. 1 5 Cleanliness . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .*. 2 6 Limits for acidity or alkalinity . . . . .*. 3 7 Limits for extractable metals . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 8 Lubricant . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 9 Tolerante on graduated capacity . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 10 Graduated scale . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 11 Barrel . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 12 Piston/plunger assembly . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 13 Nozzle . . . . . . . . . .I. 5 14 Performance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6 15 Packaging . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6 16 Labelling . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6 0 ISO 1993 All rights reserved. No part of this publication may be reproduced or utilized in any form or by any means, electronie or mechanical, including photocopying and microfilm, without per- mission in writing from the publisher. International Organization for Standardization Case Postale 56 l CH-l 211 Geneve 20 l Switzerland Printed in Switzerland ii SIST EN ISO 7886-1:2000
ISO 78864:1993(E) A Method for preparation of extracts ,.,. 8 B Test method for air leakage past Syringe Piston during aspiration, and for Separation of Piston and plunger *.,.,.,.,., 9 C Method for determination of dead space . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 11 D Test method for liquid leakage at Syringe Piston under compression . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 12 E Guidance on materials . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13 F Examples of test methods for incompatibility between syringes and injection fluids ,,.,.,.,.*. 14 G Test method for forces required to operate plunger . . . . . . . . , . . . 18 H Symbol for “do not re-use” . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 22 J Bibliography .,.,,,. 23 SIST EN ISO 7886-1:2000
Foreword ISO (the International Organization for Standardization) is a worldwide federation of national Standards bodies (ISO member bodies). The work of preparing International Standards is normally carried out through ISO technical committees. Esch member body interested in a subject for which a technical committee has been established has the right to be represented on that committee. International organizations, governmental and non-governmental, in liaison with ISO, also take part in the work. ISO collaborates closely with the International Electrotechnical Commission (IEC) on all matters of electrotechnical standardization. Draft International Standards adopted by the technical committees are circulated to the member bodies for voting. Publication as an International Standard requires approval by at least 75 % of the member bodies casting a vote. International Standard ISO 7886-1 was prepared by Technical Committee ISOJTC 84, Medical devices for injections, Sub-Committee SC 1, Syringes, needles and intravascular catheters for Single use. This first edition of ISO 7886-1 cancels and replaces ISO 7886:1984. lt was decided to divide the Standard into two Parts, ISO 7886-1 retaining essentially the scope of ISO 7886:1984, and ISO 7886-2 (in course of preparation) being applicable to sterile, Single-use syringes for use with power-driven Syringe Pumps. The major differentes between this part of ISO 7886 and ISO 7886:1984 are as follows. a) In Order to reflect the demand for syringes of sizes other than those listed in ISO 7886:1984, this part of ISO 7886 does not specify a range of Syringe sizes and allows the syringes to be marked with graduations at greater than the nominal capacity. b) An informative annex on forces required to operate the Syringe plunger has been introduced. c) The tests for toxicity given in ISO 7886:1984 have been replaced by an informative Cross-reference to ISO 10993-1. d) The informative annex on test methods for compatibility between syringes and injection fluids has been revised. e) This part of ISO 7886 permits the use on package labelling of the ISO Symbol for “do not re-use”, but continues to require the written word. Manufacturers are encouraged to use the Symbol so as to increase familiarity with it among purchasers and users. ISO 7886 consists of the following Parts, under the general title Sterile hypodermic syringes for Single use: - Part 1: Syringes for manual use iv SIST EN ISO 7886-1:2000
ISO 78864:1993(E) - Part 2: Syringes for use with Syringe Pumps Annexes A, B, C and D form an integral part of this part of ISO 7886. An- nexes E, F, G, H and J are for information only. SIST EN ISO 7886-1:2000
ISO 7886=1:1993(E) Introduction This part of ISO 7886 does not give requirements or test methods for freedom from biological hazard. Guidance on biological tests relevant to hypodermic syringes is given in ISO 10993-1, and it is suggested that manufacturers take this guidance into account when evaluating products. Such an evaluation should include the effects of the process whereby the syringes are sterilized. However, national regulations may exist in some countries, and these will override the guidance in ISO 10993-1. Materials to be used for the construction of syringes are not specified as their selection will depend to some extent upon the design, process of manufacture and method of sterilization employed by individual manufac- turers. Guidance on some aspects of the selection of materials is given in annex E. The materials of the Syringe should be compatible with injection fluids. If this is not the case, the attention of the user should be drawn to the ex- ception by labelling the primary Container. lt is not practicable to specify a universally acceptable test method for incompatibility. However, recom- mended methods are given in annex F. These test methods tan be re- garded only as a means of indicating compatibility. The only conclusive test is that of an individual injection fluid with a specific Syringe. Manufacturers of pharmaceuticals use solvents in injectable preparations. Such solvents should be tested by the manufacturer of the injectable preparation for any possible incompatibility with the materials frequently used in Syringe construction. The types of material that have received wide acceptance are included in annex E. If an incompatibility exists, the injection should be suitably labelled. The impossibility of testing any one injection fluid with all available syringes is recognized and it is strongly recommended that regulatory authorities and relevant trade associations should recognize the Problem and take appropriate measures to assist manufacturers. Hypodermic syringes specified in this part of ISO 7886 are intended for use with hypodermic needles specified in ISO 7864. This part of ISO 7886 does not cover syringes for the injection of insulin (see ISO 8537). In some countries, national pharmacopoeia or government regulations are legally binding and their requirements may take precedence over this part of ISO 7886. vi SIST EN ISO 7886-1:2000
INTERNATIONAL STANDARD ISO 7886=1:1993(E) Sterile hypodermic syringes for Single use - Part 1: Syringes for manual use 1 Scope This part of ISO 7886 specifies requirements for sterile Single-use hypodermic syringes made of plas- tics materials and intended for the aspiration of fluids or for the injection of fluids immediately after filling. lt excludes syringes for use with insulin (see ISO 8537), Single-use syringes made of glass, syringes with needles permanently attached, syringes for use with power-driven Syringe Pumps, syringes pre-filled with the injection by the manufacturer and syringes supplied with the injection as a kit for filling by a pharmaeist. NOTE 1 A second part of ISO 7886 is being prepared to cover syringes for use with power-driven Syringe Pumps. 2 Normative references The following Standards contain provisions which, through reference in this text, constitute provisions of this part of ISO 7886. At the time of publication, the editions indicated were valid. All Standards are subject to revision, and Parties to agreements based on this part of ISO 7886 are encouraged to investigate the possibility of applying the most recent editions of the Standards indicated below. Members of IEC and ISO maintain registers of currently valid International Standards. ISO 594-1: 1986, Conical fittings with a 6 % (Luer) ta- per for syringes, needles and certain other medical equipment - Part 1: General requiremen ts. ISO 594-2: 1991, Conical fittings with a 6 % (Luer) ta- per for syringes, needles and certain other medical equipment - Part 2: Lack fittings. ISO 3696: 1987, Water for analytical laboratory use - Specifica tion and test methods. ISO 8601: 1988, Data elemen ts and in terchange for- mats - Information in terchange - Represen ta tion of dates and times. 3 Definitions For the purposes of this part of ISO 7886, the follow- ing definitions apply. 3.1 nominal capacity: Capacity of the Syringe as designated by the manufacturer. NOTE 2 Examples are 1 ml, 5 ml, 50 ml. 3.2 graduated capacity: Volume of water at (20 k 5) “C [or, for tropical countries (27 + 5) “C] expelled from the Syringe when the fiducial line on the Piston traverses a given scale interval or intervals. 3.3 total graduated capacity: Capacity of the Syringe at the graduation line furthest from the zero graduation line. NOTE 3 The total graduated capacity may be equal to, or greater than, the nominal capacity. 3.4 maximum usable capacity: Capacity of the Syringe when the Piston is drawn back to its furthest functional Position. 3.5 fiducial line: Line circumscribing the end of the Piston for determining the capacity corresponding to any scale reading of the Syringe. 4 Nomenclature The nomenclature for components of hypodermic syringes for Single use is shown in figure 1. SIST EN ISO 7886-1:2000
ISO 7886=1:1993(E) 8 9 y/ 14 1. Zero graduation line 5. Fiducial line 10. Barrel 2. Graduation lines 6. Finger grips 11. Piston 3. Nominal capacity graduation line 7. Nozzle cap 12. Seal 4. Total graduated capacity line 8. Nozzle lumen 13. Plunger 9. Nozzle 14. Push-button NOTE - The drawing is intended to be illustrative of components of a Syringe. The piston/plunger assembly may or may not be of integral construction and may or may not incorporate more than one Seal. Figure 1 - Schematic representation of hypodermic Syringe for Single use 2 SIST EN ISO 7886-1:2000
ISO 7886=1:1993(E) mium content of the control fluid, be lower than 0,l mg/l. 5 Cleanliness When inspected by normal or corrected-to-normal vi- sion without magnification under an illuminance of 300 IX to 700 IX, the surface of the hypodermic Syringe which Comes in contact with injection fluids during normal use shall be free from particles and extraneous matter. 8 Lubricant If the interior surfaces of the Syringe, including the Piston, are lubricated, the lubricant shall not be visible, under normal or corrected-to-normal Vision, as drop- lets or particles. An acceptable Iubricant, applied undiluted, for three- piece syringes is polydimethylsiloxane complying with a national or the European pharmacopoeia. The quan- tity of Iubricant used should not exceed 0,25 mg per Square centimetre of the internal surface area of the Syringe barrel. 6 Limits for acidity or alkalinity When determined with a laboratoty pH meter and using a general purpose electrode, the pH value of an extract prepared in accordance with annex A shall be within one unit of pH of that of the control fluid. An acceptable lubricant for two-piece syringes is fatty ac
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