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ANSI/AAMI/IEC 80601-2-30:2018 - Medical electrical equipment-Part 2-30: Particular requirements for basic safety and essential performance of automated type non-invasive sphygmomanometers, 2018
- ANSI/AAMI/IEC 80601-2-30:2018; Medical electrical equipment—Part 2-30: Particular requirements for the basic safety and essential performance of automated type non-invasive sphygmomanometers
- Title page
- AAMI Standard
- Untitled
- Contents
- Committee representation
- Background of ANSI/AAMI adoption of IEC 80601-2-30:2018
- Foreword
- Introduction
- 201.1 Scope, object and related standards [Go to Page]
- 201.1. 1 Scope
- 201.1. 2 Object
- 201.1. 3 Collateral standards
- 201.1. 4 Particular standards
- 201.2 Normative references
- 201.3 Terms and definitions
- 201.4 General requirements [Go to Page]
- 201.4. 3 Essential performance
- 201.4. 3.101 Additional essential performance requirements [Go to Page]
- Table 201.101 – Distributed ESSENTIAL PERFORMANCE requirements
- 201.5 General requirements for testing me equipment
- 201.6 Classification of me equipment and me systems
- 201.7 Me equipment identification, marking and documents [Go to Page]
- 201.7. 2 Marking on the outside of me equipment or me equipment parts
- 201.7. 2.4 * Accessories
- 201.7. 2.101 Display of automated sphygmomanometers
- 201.7. 2.102 * Automated sphygmomanometer with neonatal mode
- 201.7. 2.103 * Automated sphygmomanometer intended for self-use in public areas
- 201.7. 2.104 * Component replacement
- 201.7. 2.105 Disposal
- 201.7. 9.2 Instructions for use
- 201.7. 9.2.1 General
- 201.7. 9.2.2 Warning and safety notices
- 201.7. 9.2.5 Me equipment description
- 201.7. 9.2.9 Operating instructions
- 201.7. 9.2.13 * Maintenance
- 201.7. 9.2.101 Compatibility with hf surgical equipment
- 201.7. 9.2.102 Automated sphygmomanometers for use in neonatal mode
- 201.8 Protection against electrical hazards from me equipment [Go to Page]
- 201.8. 5.5 Defibrillation-proof applied parts
- 201.8. 5.5.101 * Patient connections of automated sphygmomanometers
- 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 [Go to Page]
- 201.11. 8 Interruption of the power supply/supply mains to me equipment
- 201.11. 8.101 * Switching off [Go to Page]
- Table 201.102 – CUFF deflation pressure
- 201.11. 8.102 Interruption of the supply mains
- 201.11. 8.103 * Internal electrical power source
- 201.12 Accuracy of controls and instruments and protection against hazardous outputs [Go to Page]
- 201.12. 1 Accuracy of controls and instruments
- 201.12. 1.101 Measuring and display ranges
- 201.12. 1.102 Limits of the error of the manometer from environmental conditions
- 201.12. 1.103 * Nominal blood pressure indication range
- 201.12. 1.104 Maximum pressure in normal condition
- 201.12. 1.105 * Maximum pressure in single fault condition [Go to Page]
- Figure 201.101 – CUFF pressure PROTECTION DEVICE, triggered by overpressure in SINGLE FAULT CONDITION
- 201.12. 1.106 * Manometer test mode [Go to Page]
- Figure 201.102 – CUFF pressure PROTECTION DEVICE, triggered by prolonged overpressure in SINGLE FAULT CONDITION
- 201.12. 1.107 * Reproducibility of the blood pressure determination
- 201.12. 3 Alarm systems
- 201.12. 3.101 Additional alarm system requirements
- 201.13 Hazardous situations and fault conditions for me equipment
- 201.14 Programmable electrical medical systems (pems)
- 201.15 Construction of me equipment [Go to Page]
- 201.15. 3.5 Rough handling test
- 201.15. 3.5.101 * Shock and vibration (robustness)
- 201.16 Me systems
- 201.17 Electromagnetic compatibility of me equipment and me systems
- 201.101 Requirements for cuffs [Go to Page]
- 201.101. 1 * Construction
- 201.101. 2 * Pressurization
- 201.101. 3 * Automated sphygmomanometer intended for self-use in public areas with a single cuff size
- 201.102 * Connection tubing and cuff connectors
- 201.103 Unauthorized access
- 201.104 * Maximum inflating time [Go to Page]
- Table 201.103 – CUFF inflation pressure
- Figure 201.103 – CUFF pressure and maximum inflation time, NORMAL CONDITION and SINGLE FAULT CONDITION
- 201.105 * Automatic cycling modes [Go to Page]
- 201.105. 1 Long-term automatic mode [Go to Page]
- Figure 201.104 – LONG-TERM AUTOMATIC MODE CUFF pressure in NORMAL CONDITION
- Figure 201.105 – LONG-TERM AUTOMATIC MODE CUFF pressure in SINGLE FAULT CONDITION
- 201.105. 2 * Short-term automatic mode [Go to Page]
- Figure 201.106 – SHORT-TERM AUTOMATIC MODE CUFF pressure
- 201.105. 3 * Self-measurement automatic mode
- 201.105. 3.1 General [Go to Page]
- Figure 201.107 – SELF-MEASUREMENT AUTOMATIC MODE CUFF pressure
- 201.105. 3.2 Normal condition
- 201.105. 3.3 * Single fault condition
- 201.106 * Clinical accuracy
- 202 Electromagnetic disturbances – Requirements and tests [Go to Page]
- 202.4.3.1 Configurations
- 202.5.2.2.1 Requirements applicable to all me equipment and me systems
- 202.8 Electromagnetic immunity requirements for me equipment and me systems
- 202.8.1 General
- 202.8.1.101 Additional general requirements
- 202.8.101 * Electrosurgery interference recovery [Go to Page]
- Figure 202.101 – HF SURGICAL EQUIPMENT test layout
- Figure 202.102 – Simulated PATIENT test set-up for HF SURGICAL EQUIPMENT
- 206 Usability
- 210 Requirements for the development of physiologic closed-loop controllers [Go to Page]
- 210.4 General requirements
- 211 Requirements for medical electrical equipment and medical electrical systems used in the home healthcare environment [Go to Page]
- 211.4.2.2 Environmental conditions of transport and storage between uses
- 211.4.2.3.1 Continous operating conditions
- 211.7.4.5 Additional requirements for operating instructions
- 211.8.3.1 Ingress of water or particulate matter into me equipment
- 212 Requirements for medical electrical equipment and medical electrical systems intended for use in the emergency medical services environment [Go to Page]
- 212.10.1.1 General requirements for mechanical strength
- Annexes
- Annex C (informative) Guide to marking and labelling requirements for me equipment and me systems [Go to Page]
- 201.C.1 Marking on the outside of me equipment, me systems or their parts [Go to Page]
- Table 201.C.101 – Marking on the outside of AUTOMATED SPHYGMOMANOMETERS or their parts
- 201.C.3 Marking of controls and instruments [Go to Page]
- Table 201.C.102 – Marking of controls and instruments of AUTOMATED SPHYGMOMANOMETERS or their parts
- 201.C.4 Accompanying documents, general [Go to Page]
- Table 201.C.103 – ACCOMPANYING DOCUMENTS, general information for AUTOMATED SPHYGMOMANOMETERS
- 201.C.5 Accompanying documents, Instructions for use [Go to Page]
- Table 201.C.104 – ACCOMPANYING DOCUMENTS, instructions for use of AUTOMATED SPHYGMOMANOMETERS
- 201.C.6 Accompanying documents, technical description [Go to Page]
- Table 201.C.105 – ACCOMPANYING DOCUMENTS, technical description of AUTOMATED SPHYGMOMANOMETERS
- Annex AA (informative) Particular guidance and rationale
- AA.1 General guidance
- AA.2 Rationale for particular clauses and subclauses [Go to Page]
- Table AA.1 – Summary of requirements by mode
- Annex BB (informative) Environmental aspects [Go to Page]
- Table BB.1 – Environmental aspects addressed by clauses of this document
- Annex CC (informative) Reference to the essential principles [Go to Page]
- Table CC.1 – Correspondence between this particular standard and the ESSENTIAL PRINCIPLES
- Bibliography
- Index of defined terms [Go to Page]