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  • Query or request:  Areas of applications
  • Search: 09.01 - Medical devices in general
  • Hits: 108
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 No.Document numberIssuing DateTitle
61 EN ISO 23907-1 2019-02-01 Sharps injury protection - Requirements and test methods - Part 1: Single-use sharps containers (ISO 23907-1:2019)
62 IEC 62D/1759A/CD; IEC 80601-2-52 2020-05-01 Medical electrical equipment - Part 2-52: Particular requirements for the basic safety and essential performance of medical beds
63 IEC 60601-2-52 2009-12-01 Medical electrical equipment - Part 2-52: Particular requirements for basic safety and essential performance of medical beds
64 IEC 60601-2-52 Corrigendum 1 2010-09-01 Medical electrical equipment - Part 2-52: Particular requirements for the basic safety and essential performance of medical beds
65 IEC 60601-2-52 AMD 1 2015-03-01 Medical electrical equipment - Part 2-52: Particular requirements for the basic safety and essential performance of medical beds
66 IEC 61340-6-1 2018-09-01 Electrostatics - Part 6-1: Electrostatic control for healthcare - General requirements for facilities
67 IEC 62366-1 2015-02-01 Medical devices - Part 1: Application of usability engineering to medical devices
68 IEC 62366-1 Corrigendum 1 2016-07-01 Medical devices - Part 1: Application of usability engineering to medical devices; Corrigendum 1
69 IEC 62366-1 AMD 1 2020-06-01 Medical devices - Part 1: Application of usability engineering to medical devices; Amendment 1
70 IEC/TR 62366-2 2016-04-01 Medical devices - Part 2: Guidance on the application of usability engineering to medical devices
71 ISO 4073 2009-07-01 Dentistry - Information system on the location of dental equipment in the working area of the oral health care provider
72 ISO 10282 2023-02-01 Single-use sterile rubber surgical gloves - Specification
73 ISO 11137-1 2006-04-01 Sterilization of health care products - Radiation - Part 1: Requirements for development, validation and routine control of a sterilization process for medical devices
74 ISO/DIS 11137-1 2023-04-01 Sterilization of health care products - Radiation - Part 1: Requirements for the development, validation and routine control of a sterilization process for medical devices
75 ISO 11137-1 AMD 1 2013-07-01 Sterilization of health care products - Radiation - Part 1: Requirements for development, validation and routine control of a sterilization process for medical devices; Amendment 1
76 ISO 11137-1 AMD 2 2018-11-01 Sterilization of health care products - Radiation - Part 1: Requirements for development, validation and routine control of a sterilization process for medical devices - Amendment 2: Revision to 4.3.4 and 11.2
77 ISO 11137-2 2013-06-01 Sterilization of health care products - Radiation - Part 2: Establishing the sterilization dose
78 ISO 11137-2 AMD 1 2022-06-01 Sterilization of health care products - Radiation - Part 2: Establishing the sterilization dose; Amendment 1
79 ISO 11137-3 2017-06-01 Sterilization of health care products - Radiation - Part 3: Guidance on dosimetric aspects of development, validation and routine control
80 ISO 11138-1 2017-03-01 Sterilization of health care products - Biological indicators - Part 1: General requirements

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