SIST EN 1282-2:2005+A1:2009
(Main)Tracheostomy tubes - Part 2: Paediatric tubes (ISO 5366-3:2001, modified)
Tracheostomy tubes - Part 2: Paediatric tubes (ISO 5366-3:2001, modified)
This European Standard specifies requirements for paediatric tracheostomy tubes made of plastics materials and/or rubber having inside diameters from 2,0 mm to 6,0 mm. Requirements for paediatric tracheostomy tube connectors and adaptors are also given.
This document is not applicable to specialized tracheostomy tubes.
Tracheotomietuben - Teil 2: Pädiatrische Tuben (ISO 5366-3:2001, geändert)
Diese Europäische Norm legt Anforderungen an pädiatrische Tracheotomietuben aus Kunststoffen und/oder Gummi mit einem Innendurchmesser von 2,0 mm bis 6,0 mm fest. Es enthält auch Anforderungen an Verbindungsstücke und Adapter für pädiatrische Tracheotomietuben. Spezial-Tracheotomietuben gehören nicht zum Anwendungsbereich dieses Dokuments.
Tubes de trachéostomie - Partie 2: Tubes pédiatriques (ISO 5366-3:2001, modifiée)
Traheostomske cevke - 2. del: Cevke, ki se uporabljajo pri otrocih (ISO 5366-3:2001, spremenjen)
General Information
Relations
Standards Content (Sample)
2003-01.Slovenski inštitut za standardizacijo. Razmnoževanje celote ali delov tega standarda ni dovoljeno.Traheostomske cevke - 2. del: Cevke, ki se uporabljajo pri otrocih (ISO 5366-3:2001, spremenjen)Tracheotomietuben - Teil 2: Pädiatrische Tuben (ISO 5366-3:2001, geändert)Tubes de trachéostomie - Partie 2: Tubes pédiatriques (ISO 5366-3:2001, modifiée)Tracheostomy tubes - Part 2: Paediatric tubes (ISO 5366-3:2001, modified)11.040.10Anestezijska, respiratorna in reanimacijska opremaAnaesthetic, respiratory and reanimation equipmentICS:Ta slovenski standard je istoveten z:EN 1282-2:2005+A1:2009SIST EN 1282-2:2005+A1:2009en,de01-oktober-2009SIST EN 1282-2:2005+A1:2009SLOVENSKI
STANDARD
SIST EN 1282-2:2005+A1:2009
EUROPEAN STANDARD NORME EUROPÉENNE EUROPÄISCHE NORM
EN 1282-2:2005+A1
August 2009 ICS 11.040.10 Supersedes EN 1282-2:2005English Version
Tracheostomy tubes - Part 2: Paediatric tubes (ISO 5366-3:2001, modified)
Tubes de trachéostomie - Partie 2: Tubes pédiatriques (ISO 5366-3:2001, modifiée)
Tracheotomietuben - Teil 2: Pädiatrische Tuben (ISO 5366-3:2001, geändert) This European Standard was approved by CEN on 25 April 2005 and includes Amendment 1 approved by CEN on 16 July 2009.
CEN members are bound to comply with the CEN/CENELEC Internal Regulations which stipulate the conditions for giving this European Standard the status of a national standard without any alteration. Up-to-date lists and bibliographical references concerning such national standards may be obtained on application to the CEN Management Centre or to any CEN member.
This European Standard exists in three official versions (English, French, German). A version in any other language made by translation under the responsibility of a CEN member into its own language and notified to the CEN Management Centre has the same status as the official versions.
CEN members are the national standards bodies of Austria, Belgium, Bulgaria, Cyprus, Czech Republic, Denmark, Estonia, Finland, France, Germany, Greece, Hungary, Iceland, Ireland, Italy, Latvia, Lithuania, Luxembourg, Malta, Netherlands, Norway, Poland, Portugal, Romania, Slovakia, Slovenia, Spain, Sweden, Switzerland and United Kingdom.
EUROPEAN COMMITTEE FOR STANDARDIZATION
COMITÉ EUROPÉEN DE NORMALISATION EUROPÄISCHES KOMITEE FÜR NORMUNG
Management Centre:
Avenue Marnix 17,
B-1000 Brussels © 2009 CEN All rights of exploitation in any form and by any means reserved worldwide for CEN national Members. Ref. No. EN 1282-2:2005+A1:2009: ESIST EN 1282-2:2005+A1:2009
EN 1282-2:2005+A1:2009 (E) 2 Contents Page Foreword .3 Introduction .4 1 Scope .5 2 Normative references .5 3 Terms and definitions .5 4 Size designation and dimensions .6 4.1 Designation of size of tube .6 4.2 Outside diameter.6 4.3 Length .7 4.4 Angle
....................................................................................................................................................8 5 Materials .................................................................................................................................................8 6 Design and finish ...................................................................................................................................8 6.1 Machine end ...........................................................................................................................................8 6.2 Paediatric tracheostomy tube connector ............................................................................................8 6.3 Inner tube ................................................................................................................................................9 6.4 Neck-plate ............................................................................................................................................ 10 6.5 Cuff ....................................................................................................................................................... 10 6.6 Inflating tubes for cuffs ...................................................................................................................... 10 6.7 Patient end ........................................................................................................................................... 10 6.8 Introducer ............................................................................................................................................ 10 7 Requirements for tracheostomy tubes supplied sterile ................................................................. 11 7.1 Sterility assurance .............................................................................................................................. 11 7.2 Packaging for tracheostomy tubes supplied sterile ....................................................................... 11 8 Marking ................................................................................................................................................ 11 8.1 Marking of tracheostomy tube .......................................................................................................... 11 8.2 Marking of tracheostomy tube connectors ...................................................................................... 11 8.3 Marking of unit packs ......................................................................................................................... 11 9 Adaptor ................................................................................................................................................ 13 Annex A (normative)
Test for security of attachment of permanently attached connector, if provided, and neck-plate to tracheostomy tube . 14 A.1 Principle . 14 A.2 Apparatus . 14 A.3 Procedure . 14 A.4 Expression of results . 15 Annex B (normative)
Test method for determining the resting diameter of the cuff . 16 B.1 Principle . 16 B.2 Apparatus . 16 B.3 Procedure . 16 B.4 Expression of results . 16 Annex C (informative)
Guidance on materials and design . 17 C.1 Materials . 17 C.2 Design . 17 Annex ZA (informative)
Relationship between this European Standard and the Essential Requirements of EU Directive 93/42/EEC Medical devices . 18 Bibliography . 20
SIST EN 1282-2:2005+A1:2009
EN 1282-2:2005+A1:2009 (E) 3 Foreword The text of the International Standard ISO 5366-3:2001, including Corrigendum 1:2003 from Technical Committee ISO/TC 121 “Anaesthetic and respiratory equipment” of the International Organization for Standardization (ISO) has been taken over as a European Standard by Technical Committee CEN/TC 215 “Respiratory and anaesthetic equipment”, the secretariat of which is held by BSI, with common modifications which are indicated by a straight line in the margin of the text. This European Standard shall be given the status of a national standard, either by publication of an identical text or by endorsement, at the latest by February 2010 and conflicting national standards shall be withdrawn at the latest by March 2010. Attention is drawn to the possibility that some of the elements of this document may be the subject of patent rights. CEN [and/or CENELEC] shall not be held responsible for identifying any or all such patent rights. This European Standard was approved by CEN on 25 April 2005 and includes Amendment 1 approved by CEN on 16 July 2009. This document supersedes !EN 1282-2:2005". The start and finish of text introduced or altered by amendment is indicated in the text by tags !". This document has been prepared under a mandate given to CEN by the European Commission and the European Free Trade Association, and supports essential requirements of EU Directive(s). For relationship with EU Directive(s), see informative Annex ZA, which is an integral part of this document. According to the CEN/CENELEC Internal Regulations, the national standards organizations of the following countries are bound to implement this European Standard: Austria, Belgium, Bulgaria, Cyprus, Czech Republic, Denmark, Estonia, Finland, France, Germany, Greece, Hungary, Iceland, Ireland, Italy, Latvia, Lithuania, Luxembourg, Malta, Netherlands, Norway, Poland, Portugal, Romania, Slovakia, Slovenia, Spain, Sweden, Switzerland and United Kingdom.
SIST EN 1282-2:2005+A1:2009
EN 1282-2:2005+A1:2009 (E) 4 Introduction ISO 5366 is concerned with the basic requirements and method of size designation of tracheostomy tubes made of plastics materials and/or rubber. EN ISO 5366-1 gives requirements for adult tracheostomy tubes made of plastics materials and/or rubber. This document gives requirements for paediatric tracheostomy tubes with an inside diameter from 2,0 mm to 6,0 mm. Paediatric tracheostomy tubes are primarily intended for use with infants and children who may require anaesthesia, artificial ventilation, relief of upper airway obstruction or other respiratory therapy. An infant or child differs from an adult, not only in size but especially with regard to airway anatomy and respiratory physiology; thus airway equipment for paediatric patients differs from that for adults in size and also in basic design. It should be noted that, although this document gives some requirements for cuffs, cuffs are seldom provided on the smaller sizes of paediatric tubes. This document gives requirements for those characteristics of tracheostomy tubes that can be standardized and which are important for patient safety. It does not require the connector to be permanently attached to the tube, as this may be impractical with infants and small children. Other acceptable methods of connecting these components are available, and this document makes provision for them. This document does not limit the range of tube designs needed to match the variety of paediatric anatomy, lesions and space limitations encountered. The method of describing tube dimensions and configuration has been devised with the aim of assisting the clinician in the selection of a suitable tube to conform as far as possible to a particular patient's anatomy. Size is designated by inside diameter, which is important because of its relation to resistance to gas flow. Because the stomal and tracheal diameters are important when selecting tubes, it is considered essential that the outside diameter be stated for each size of tube. A tracheostomy tube can increase resistance to gas flow. For tubes with a given outside diameter, differences in wall thickness have a major influence on the resistance to gas flow, especially in the smaller sizes of paediatric tracheostomy tubes. Flammability of tracheostomy tubes, for example if flammable anaesthetics, electrosurgical units or lasers are used in oxidant-enriched atmospheres, is a well-recognized hazard1 addressed by appropriate clinical management, which is outside the scope of this document.
1See ISO/TR 11991. SIST EN 1282-2:2005+A1:2009
EN 1282-2:2005+A1:2009 (E) 5 1 Scope This European Standard specifies requirements for paediatric tracheostomy tubes made of plastics materials and/or rubber having inside diameters from 2,0 mm to 6,0 mm. Requirements for paediatric tracheostomy tube connectors and adaptors are also given. This document is not applicable to specialized tracheostomy tubes. 2 Normative references The following referenced documents are indispensable for the application of this document. For dated references, only the edition cited applies. For undated references, the latest edition of the referenced document (including any amendments) applies. EN 556-1:2001, Sterilization of medical devices — Requirements for medical devices to be labelled “STERILE” EN ISO 5356-1, Anaesthetic and respiratory equipment — Conical connectors — Part 1: Cones and sockets (ISO 5356-1:2004) EN ISO 5366-1:2004, Anaesthetic and respiratory equipment — Tracheostomy tubes — Part 1: Tubes and connectors for use in adults (ISO 5366-1:2000) EN ISO 10993-1, Biological evaluation of medical devices — Part 1: Evaluation and testing (ISO 10933-1:2003) EN 20594-1, Conical fittings with a 6 % (Luer) taper for syringes, needles and certain other medical equipment — Part 1: General requirements ISO 5361, Anaesthetic and respiratory equipment — Tracheal tubes and connectors ISO 11607, Packaging for terminally sterilized medical devices 3 Terms and definitions For the purposes of this European Standard, the terms and definitions given in EN ISO 5366-1:2004 and the following apply. 3.1 paediatric tracheostomy tube tube designed for insertion into the trachea of an infant or child through a tracheostomy 3.2 paediatric tracheostomy tube connector tubular component which fits directly into the paediatric tracheostomy tube 3.3 machine end (paediatric tracheostomy tube connector) end of the component nearest the machine which is intended to mate with the breathing system of an anaesthetic machine or lung ventilator 3.4 patient end (paediatric tracheostomy tube connector) end of the component nearest the patient which is inserted into the paediatric tracheostomy tube SIST EN 1282-2:2005+A1:2009
EN 1282-2:2005+A1:2009 (E) 6 3.5 adaptor specialized connector to establish functional continuity between otherwise disparate or incompatible components 4 Size designation and dimensions 4.1 Designation of size of tube 4.1.1 The size of a tracheostomy tube (outer tube) shall be designated by the nominal inside diameter (ID) of the tube expressed in millimetres, as measured at the minimum diameter, in accordance with Table 1, excluding any encroachment allowed by 6.6.1. 4.1.2 For tracheostomy tubes provided with an inner tube to which is attached an 8,5 mm or 15 mm male conical connector complying with the requirements of EN ISO 5356-1 [see 6.1 a)], the size shall be designated by the nominal inside diameter (ID) of the inner tube expressed in millimetres in accordance with Table 1. Table 1 — Size designation, inside diameter and tolerances of paediatric tracheostomy tubes
Dimensions in millimetres
Designated size Inside diameterTolerance
2,0 2,0 +0,2 0
2,5 2,5
3,0 3,0
3,5 3,5
4,0 4,0
4,5 4,5 + 0,3 0
5,0 5,0
5,5 5,5
6,0 6,0 4.2 Outside diameter 4.2.1 The outside diameter (OD) of sections A and C (see Figure 1) of the tube, other than at the cuff if provided, shall be expressed in millimetres to the nearest 0,1 mm. NOTE
The marked outside diameter relates to that portion of the tube intended to be within the wall and lumen of the trachea. 4.2.2 The actual outside diameter of section A, other than at the cuff if provided, shall be the marked outside diameter subject to a tolerance of ± 0,2 mm. 4.2.3 The actual outside diameter of section C shall be the marked outside diameter subject to a tolerance of
± 0,5 mm. SIST EN 1282-2:2005+A1:2009
EN 1282-2:2005+A1:2009 (E) 7
a) Paediatric tracheostomy tube
b) Patient end Key 1
Neck-plate 2
Datum plane 3
Tip rounded 4
Bevel, if present a Obtuse angle formed between the long axes of the tube at the machine and patient ends. Figure 1 — Basic dimensions of paediatric tracheostomy tubes 4.3 Length 4.3.1 The nominal length (l1 + l2 + l3 in Figure 1) shall be measured from the patient side of the neck-plate to the patient end, including the bevel if present (see Figure 1), and expressed in millimetres. 4.3.2 The actual nominal length (l1 + l2 + l3 in Figure 1) shall be the marked nominal length subject to a tolerance of ± 1,5 mm for tubes with a marked inside diameter of less than 4,5 mm, or subject to a tolerance of ± 2 mm for tubes with a marked inside diameter of 4,5 mm or greater. SIST EN 1282-2:2005+A1:2009
EN 1282-2:2005+A1:2009 (E) 8 4.3.3 For tubes with an adjustable neck-plate, the range of measurements for nominal length (see Figure 1) shall be expressed in millimetres. 4.3.4 Dimensions l1, l2 and l3 shall be expressed in millimetres [see Figure 1 a)]. NOTE
Dimensions l1 and/or l2 can be, or approach, zero. 4.4 Angle
The angle
(see Figure 1) shall be expressed in degrees. 5 Materials Tracheostomy tubes, including cuffs and tracheostomy tube connectors provided with the tube, in their ready-for-use state after any preparation for use recommended by the manufacturer, shall satisfy appropriate biological safety testing, as indicated in EN ISO 10993-1. !NOTE 1" See Annex C for guidance on materials and design. !If phthalates are incorporated in parts
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