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| BS 5724-2.14:1989* IEC 60601-2-14:1989 | Medical electrical equipment. Particular requirements for safety. Specification for electroconvulsive therapy equipment |
| BS 5724-2.5:1985* IEC 60601-2-5:1984 | Medical electrical equipment. Particular requirements for safety. Specification for safety of ultrasonic therapy equipment |
| BS 5724-2.6:1985* IEC 60601-2-6:1984 | Medical electrical equipment. Particular requirements for safety. Specification for microwave therapy equipment |
| BS 5724-3.129:Supplement No. 1:1994* IEC 61170:1993 | Medical electrical equipment. Particular requirements for performance. Methods of declaring functional performance characteristics of radiotherapy simulators. Guide to functional performance values |
| BS 5724:Part 2:Section 2.16:1989* IEC 60601-2-16:1989 | Medical electrical equipment. Particular requirements for safety. Specification for haemodialysis equipment |
| BS EN 60601-2-17/A1:1996* BS 5724-2.17/Supplement 1:1996* IEC 60601-2-17:Amd 1:1996 | Medical electrical equipment. Particular requirements for safety. Revised and additional text |
| BS EN 60601-2-17:2004 | Medical electrical equipment. Particular requirements for the safety of automatically-controlled brachytherapy afterloading equipment |
| BS EN 60601-2-21:1995* BS 5724-2.121:1995* IEC 60601-2-21:1994 | Medical electrical equipment. Particular requirements for safety. Specification for infant radiant warmers |
| BS EN 60601-2-22:1993* BS 5724:Section 2.122:1993 * IEC 60601-2-22:1992 | Medical electrical equipment. Particular requirements for safety. Specification for diagnostic and therapeutic laser equipment |
| BS EN 60601-2-22:1996* BS 5724-2.122:1996* IEC 60601-2-22:1995 | Medical electrical equipment. Particular requirements for safety. Specification for diagnostic and therapeutic laser equipment |
| BS EN 60601-2-29/A1:1997* BS 5724-2. 129:Supplement1:1997* IEC 60601-2-29:1993/AMD 1:1996 | Medical electrical equipment. Particular requirements for safety. Specification for radiotherapy simulators. Revised and additional text |
| BS EN 60601-2-29:1996 | Medical electrical equipment. Particular requirements for safety. Specification for radiotherapy simulators |
| BS EN 60601-2-36:1997* BS 5724-2.36:1997* IEC 60601-2-36:1997 | Medical electrical equipment. Particular requirements for safety. Specification for equipment for extra-corporeally induced lithotripsy |
| BS EN 60601-2-3:1993* BS 5724-2.3:1992* IEC 60601-2-3:1991 | Medical electrical equipment. Particular requirements for safety. Specification for short-wave therapy equipment |
| BS EN 60601-2-5:2001 | Medical electrical equipment. Particular requirements for safety. Particular requirements for the safety of ultrasonic physiotherapy equipment |
| BS EN 61168:1994* BS 5724-3.129:1994* IEC 61168:1993 | Medical electrical equipment. Particular requirements for performance. Methods of declaring functional performance characteristics of radiotherapy simulators |
| BS EN 61689:1997* IEC 61689:1996 | Ultrasonics. Physiotherapy systems. Performance requirements and methods of measurement in the frequency range 0.5 MHz to 5 MHz |
| BS EN 61689:2007 | Ultrasonics. Physiotherapy systems. Field specifications and methods of measurement in the frequency range 0,5 MHz to 5 MHz |
| BS EN 61828:2002* IEC 61828:2001 | Ultrasonics. Focusing transducers. Definitions and measurement methods for the transmitted fields |
| BS EN 61846:1999* IEC 61846:1998 | Ultrasonics. Pressure pulse lithotripters. Characteristics of fields |
| BS EN 62083:2001* IEC 62083:2000 | Medical electrical equipment. Requirements for the safety of radiotherapy treatment planning systems |
| BS EN 62274:2005 | Medical electrical equipment. Safety of radiotherapy record and verify systems |
| PAS 83:2006 | Guidance on codes of practice, standardised methods and regulations for cell-based therapeutics |
| PD CR 13903:2001 | General guidance on the equipment used for inhaled nitric oxide therapy |
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