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withdrawn: DIN EN 60601-2-16 VDE 0750-2-16:2016-02Medical electrical equipment Part 2-16: Particular requirements for the basic safety and essential performance of haemodialysis, haemodiafiltration and haemofiltration equipment |
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withdrawn: DIN EN 60601-2-26 VDE 0750-2-26:2016-02Medical electrical equipment Part 2-26: Particular requirements for the basic safety and essential performance of electroencephalographs |
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withdrawn: DIN EN 80601-2-30 VDE 0750-2-30:2016-02Medical electrical equipment Part 2-30: Particular requirements for the basic safety and essential performance of automated non-invasive sphygmomanometers |
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DIN EN 60601-2-47 VDE 0750-2-47:2016-02Medical electrical equipment Part 2-47: Particular requirements for the basic safety and essential performance of ambulatory electrocardiographic systems |
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DIN EN 45502-1 VDE 0750-10:2016-02Implants for surgery – Active implantable medical devices Part 1: General requirements for safety, marking and for information to be provided by the manufacturer; |
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withdrawn: DIN EN 60601-1-12 VDE 0750-1-12:2016-01Medical electrical equipment Part 1-12: General requirements for basic safety and essential performance – Collateral Standard: Requirements for medical electrical equipment and medical electrical systems intended for use in the emergency medical services environment |
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withdrawn: DIN EN 60601-2-10 VDE 0750-2-10:2015-11Medical electrical equipment Part 2-10: Particular requirements for the basic safety and essential performance of nerve and muscle stimulators |
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DIN EN 60601-2-36 VDE 0750-2-36:2015-11Medical electrical equipment Part 2-36: Particular requirements for the basic safety and essential performance of equipment for extracorporeally induced lithotripsy |
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withdrawn: DIN EN 80601-2-58 VDE 0750-2-58:2015-11Medical electrical equipment Part 2-58: Particular requirements for the basic safety and essential performance of lens removal devices and vitrectomy devices for ophthalmic surgery |
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DIN EN 62353 VDE 0751-1:2015-10Medical electrical equipment Recurrent test and test after repair of medical electrical equipment |
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withdrawn: DIN EN 60601-2-22 VDE 0750-2-22:2015-08Medical electrical equipment Part 2-22: Particular requirements for basic safety and essential performance of surgical, cosmetic, therapeutic and diagnostic laser equipment |
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DIN EN 60601-2-27 VDE 0750-2-27:2015-04Medical electrical equipment Part 2-27: Particular requirements for the basic safety and essential performance of electrocardiographic monitoring equipment |
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DIN EN 60601-2-34 VDE 0750-2-34:2015-01Medical electrical equipment Part 2-34: Particular requirements for the basic safety and essential performance of invasive blood pressure monitoring equipment |
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withdrawn: DIN EN 60601-2-44 VDE 0750-2-44:2014-11Medical electrical equipment Part 2-44: Particular requirements for the basic safety and essential performance of X-ray equipment for computed tomography An english translation of this document is available. |
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withdrawn: DIN EN 60601-1-3 VDE 0750-1-3:2014-06Medical electrical equipment Part 1-3: General requirements for basic safety and essential performance – Collateral Standard: Radiation protection in diagnostic X-ray equipment |
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withdrawn: DIN EN 60601-1-9 VDE 0750-1-9:2014-05Medical electrical equipment Part 1-9: General requirements for basic safety and essential performance |
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withdrawn: DIN EN 60601-1-8 VDE 0750-1-8:2014-04Medical electrical equipment Part 1-8: General requirements for basic safety and essential performance – Collateral Standard: General requirements, tests and guidance for alarm systems in medical electrical equipment and medical electrical systems |
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DIN EN 60601-2-2 VDE 0750-2-2 Beiblatt 1:2014-02Medical electrical equipment Part 2-2: Particular requirements for basic safety and essential performance of high frequency surgical equipment and high frequency surgical accessories – Supplement 1: High frequency surgical equipment – Operation and maintenance An english translation of this document is available. |
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withdrawn: DIN EN 60601-1 VDE 0750-1:2013-12Medical electrical equipment Part 1: General requirements for basic safety and essential performance |
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withdrawn: DIN EN 61689 VDE 0754-3:2013-12Ultrasonics Physiotherapy systems - Field specifications and methods of measurement in the frequency range 0,5 MHz to 5 MHz |