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IEC 60601-2-3 Ed. 3.2 b:2022 Medical electrical equipment - Part 2-3: Particular requirements for the basic safety and essential performance of short-wave therapy equipment, 2022
- Redline version [Go to Page]
- English [Go to Page]
- CONTENTS
- FOREWORD
- INTRODUCTION
- INTRODUCTION to Amendment 2
- 201.1 Scope, object and related standards
- 201.2 Normative references
- 201.3 Terms and definitions
- 201.4 General requirements
- 201.5 General requirements for testing of me equipment
- 201.6 Classification of me equipment and me systems
- 201.7 Me equipment identification, marking and documents
- 201.8 Protection against electrical hazards from me equipment
- 201.9 Protection against mechanical hazards of me equipment and me systems
- 201.10 Protection against unwanted and excessive radiation hazards
- 201.11 Protection against excessive temperatures and other hazards
- 201.12 Accuracy of controls and instruments and protection against hazardous outputs
- 201.13 Hazardous situations and fault conditions for me equipment
- 201.14 Programmable electrical medical systems (pems)
- 201.15 Construction of me equipment
- 201.16 Me systems
- 201.17 Electromagnetic compatibility of me equipment and me systems
- Annexes
- Annex C (informative) Guide to marking and labelling requirements for me equipment and me systems
- Annex AA (informative) Particular guidance and rationale
- Index of defined terms used in this particular standard
- Figure 201.101 – Dielectric strength test for capacitive applicators
- Figure 201.102 – Test probe
- Figure 201.103 – Dielectric strength test for inductive applicators
- Table 201.C.101 – Marking on the outside of short-wave therapy equipment or its parts
- Français [Go to Page]
- SOMMAIRE
- AVANT-PROPOS
- INTRODUCTION
- INTRODUCTION à l’Amendement 2
- 201.1 Domaine d'application, objet et normes connexes
- 201.2 Références normatives
- 201.3 Termes et définitions
- 201.4 Exigences générales
- 201.5 Exigences générales relatives aux essais des appareils em
- 201.6 Classification des appareils em et des systèmes em
- 201.7 Identification, marquage et documentation des appareils em
- 201.8 Protection contre les dangers d'origine électrique provenant des appareils em
- 201.9 Protection contre les dangers mécaniques des appareils em et systèmes em
- 201.10 Protection contre les dangers dus aux rayonnements involontaires et excessifs
- 201.11 Protection contre les températures excessives et les autres dangers
- 201.12 Précision des commandes, des instruments et protection contre les caractéristiques de sortie présentant des dangers
- 201.13 Situations dangereuses et conditions de défaut pour les appareils em
- 201.14 Systèmes électromédicaux programmables (semp)
- 201.15 Construction de l’appareil em
- 201.16 Systèmes em
- 201.17 Compatibilité électromagnétique des appareils em et des systèmes em
- Annexes
- Annexe C (informative) Guide pour le marquage et exigences d’étiquetage pour les appareils em et les systèmes em
- Annexe AA (informative) Guide particulier et justifications
- Index des termes définis utilisés dans la présente norme particulière
- Figure 201.101 – Essai de tension de tenue des applicateurs capacitifs
- Figure 201.102 – Sonde d’essai
- Figure 201.103 – Essai de tension de tenue des applicateurs inductifs
- Tableau 201.C.101 – Marquage sur l’extérieur des appareils de thérapie à ondes courtes ou de leurs parties
- Final version [Go to Page]
- English [Go to Page]
- CONTENTS
- FOREWORD
- INTRODUCTION
- INTRODUCTION to Amendment 2
- 201.1 Scope, object and related standards
- 201.2 Normative references
- 201.3 Terms and definitions
- 201.4 General requirements
- 201.5 General requirements for testing of me equipment
- 201.6 Classification of me equipment and me systems
- 201.7 Me equipment identification, marking and documents
- 201.8 Protection against electrical hazards from me equipment
- 201.9 Protection against mechanical hazards of me equipment and me systems
- 201.10 Protection against unwanted and excessive radiation hazards
- 201.11 Protection against excessive temperatures and other hazards
- 201.12 Accuracy of controls and instruments and protection against hazardous outputs
- 201.13 Hazardous situations and fault conditions for me equipment
- 201.14 Programmable electrical medical systems (pems)
- 201.15 Construction of me equipment
- 201.16 Me systems
- 201.17 Electromagnetic compatibility of me equipment and me systems
- Annexes
- Annex C (informative) Guide to marking and labelling requirements for me equipment and me systems
- Annex AA (informative) Particular guidance and rationale
- Index of defined terms used in this particular standard
- Figure 201.101 – Dielectric strength test for capacitive applicators
- Figure 201.102 – Test probe
- Figure 201.103 – Dielectric strength test for inductive applicators
- Table 201.C.101 – Marking on the outside of short-wave therapy equipment or its parts
- Français [Go to Page]
- SOMMAIRE
- AVANT-PROPOS
- INTRODUCTION
- INTRODUCTION à l’Amendement 2
- 201.1 Domaine d'application, objet et normes connexes
- 201.2 Références normatives
- 201.3 Termes et définitions
- 201.4 Exigences générales
- 201.5 Exigences générales relatives aux essais des appareils em
- 201.6 Classification des appareils em et des systèmes em
- 201.7 Identification, marquage et documentation des appareils em
- 201.8 Protection contre les dangers d'origine électrique provenant des appareils em
- 201.9 Protection contre les dangers mécaniques des appareils em et systèmes em
- 201.10 Protection contre les dangers dus aux rayonnements involontaires et excessifs
- 201.11 Protection contre les températures excessives et les autres dangers
- 201.12 Précision des commandes, des instruments et protection contre les caractéristiques de sortie présentant des dangers
- 201.13 Situations dangereuses et conditions de défaut pour les appareils em
- 201.14 Systèmes électromédicaux programmables (semp)
- 201.15 Construction de l’appareil em
- 201.16 Systèmes em
- 201.17 Compatibilité électromagnétique des appareils em et des systèmes em
- Annexes
- Annexe C (informative) Guide pour le marquage et exigences d’étiquetage pour les appareils em et les systèmes em
- Annexe AA (informative) Guide particulier et justifications
- Index des termes définis utilisés dans la présente norme particulière
- Figure 201.101 – Essai de tension de tenue des applicateurs capacitifs
- Figure 201.102 – Sonde d’essai
- Figure 201.103 – Essai de tension de tenue des applicateurs inductifs
- Tableau 201.C.101 – Marquage sur l’extérieur des appareils de thérapie à ondes courtes ou de leurs parties [Go to Page]