VDE 0750-1 : 2013
Superseded
Superseded
A superseded Standard is one, which is fully replaced by another Standard, which is a new edition of the same Standard.
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MEDICAL ELECTRICAL EQUIPMENT - PART 1: GENERAL REQUIREMENTS FOR BASIC SAFETY AND ESSENTIAL PERFORMANCE (IEC 60601-1:2005 + COR.:2006 + COR.:2007 + A1:2012)
Published date
12-01-2013
Publisher
Superseded date
09-11-2022
Superseded by
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| DevelopmentNote |
Supersedes VDE 0750. (03/2015)
|
| DocumentType |
Standard
|
| PublisherName |
Verband Deutscher Elektrotechniker
|
| Status |
Superseded
|
| SupersededBy | |
| Supersedes |
| Standards | Relationship |
| IEC 60601-1:2005+AMD1:2012 CSV | Identical |
| EN 60601-1:2006/A12:2014 | Identical |
| DIN EN 60601-1:2013-12 | Identical |
| DIN VDE 0750-1 : 1991 | Identical |
| DIN EN 60601-1 : 2010-05 | Corresponds |
| DIN EN ISO 10524-4:2008-09 | PRESSURE REGULATORS FOR USE WITH MEDICAL GASES - PART 4: LOW-PRESSURE REGULATORS |
| DIN EN 60601-2-30 : 2000 | MEDICAL ELECTRICAL EQUIPMENT - PART 2-30: PARTICULAR REQUIREMENTS FOR THE SAFETY, INCLUDING ESSENTIAL PERFORMANCE, OF AUTOMATIC CYCLING NON-INVASIVE BLOOD PRESSURE MONITORING EQUIPMENT |
| DIN 12650-1:1978-07 | MECHANICAL, PHYSICAL AND ELECTRICAL LABORATORY APPARATUS - PISTON OPERATED VOLUMETRIC APPARATUS, GENERAL REQUIREMENTS, DEFINITIONS |
| DIN ISO 14835-1:2005-12 | MECHANICAL VIBRATION AND SHOCK - COLD PROVOCATION TESTS FOR THE ASSESSMENT OF PERIPHERAL VASCULAR FUNCTION - PART 1: MEASUREMENT AND EVALUATION OF FINGER SKIN TEMPERATURE |
| DIN EN ISO 8835-3:2011-02 | INHALATIONAL ANAESTHESIA SYSTEMS - PART 3: TRANSFER AND RECEIVING SYSTEMS OF ACTIVE ANAESTHETIC GAS SCAVENGING SYSTEMS |
| DIN VDE 0750-222 : 1990 | MEDICAL ELECTRICAL EQUIPMENT; PARTICULAR REQUIREMENTS FOR THE SAFETY OF THERAPEUTIC X-RAY GENERATORS |
| DIN 58946-5:1987-01 | STERILIZATION - STEAM-STERILIZERS, SMALL-STERILIZERS, REQUIREMENTS |
| DIN EN ISO 10524-1:2006-05 | PRESSURE REGULATORS FOR USE WITH MEDICAL GAS - PART 1: PRESSURE REGULATORS AND PRESSURE REGULATORS WITH FLOW-METERING DEVICES |
| DIN EN 60601-2-40 : 1998 | MEDICAL ELECTRICAL EQUIPMENT - PART 2-40: PARTICULAR REQUIREMENTS FOR THE SAFETY OF ELECTROMYGRAPHS AND EVOKED RESPONSE EQUIPMENT |
| DIN EN ISO 17510-1:2009-07 | Sleep apnoea breathing therapy - Part 1: Sleep apnoea breathing therapy equipment (ISO 17510-1:2007) |
| DIN EN ISO 21969:2010-04 | High-pressure flexible connections for use with medical gas systems (ISO 21969:2009) |
| DIN EN ISO 7376:2010-01 | ANAESTHETIC AND RESPIRATORY EQUIPMENT - LARYNGOSCOPES FOR TRACHEAL INTUBATION |
| DIN EN ISO 11143:2008-10 | DENTISTRY - AMALGAM SEPARATORS |
| DIN EN 793 : 1998 | PARTICULAR REQUIREMENTS FOR SAFETY OF MEDICAL SUPPLY UNITS |
| DIN EN 60601-2-35 : 1997 | MEDICAL ELECTRICAL EQUIPMENT - PART 2: PARTICULAR REQUIREMENTS FOR THE SAFETY OF BLANKETS, PADS AND MATTRESSES, INTENDED FOR HEATING IN MEDICAL USE |
| DIN EN ISO 26782:2010-02 | Anaesthetic and respiratory equipment - Spirometers intended for the measurement of time forced expired volumes in humans (ISO 26782:2009 + Cor. 1:2009) (includes Corrigendum AC:2009) |
| DIN EN ISO 80601-2-72:2016-04 | Medical electrical equipment - Part 2-72: Particular requirements for basic safety and essential performance of home healthcare environment ventilators for ventilator-dependent patients (ISO 80601-2-72:2015) |
| DIN 13402:1977-03 | MEDICAL ELECTRONIC TEMPERATURE METER |
| DIN EN ISO 22665:2013-04 | OPHTHALMIC OPTICS AND INSTRUMENTS - INSTRUMENTS TO MEASURE AXIAL DISTANCES IN THE EYE (ISO 22665:2012) |
| DIN EN ISO 15002:2008-11 | FLOW-METERING DEVICES FOR CONNECTION TO TERMINAL UNITS OF MEDICAL GAS PIPELINE SYSTEMS |
| DIN EN 61010-2-031 : 1995 | SAFETY REQUIREMENTS FOR ELECTRICAL EQUIPMENT FOR MEASUREMENT, CONTROL AND LABORATORY USE - PART 2-031: PARTICULAR REQUIREMENTS FOR HAND-HELD PROBE ASSEMBLIES FOR ELECTRICAL MEASUREMENT AND TEST |
| DIN EN ISO 81060-1:2012-08 | Non-invasive sphygmomanometers - Part 1: Requirements and test methods for non-automated measurement type (ISO 81060-1:2007) |
| DIN 6853-1 : 92 AMD 1 98 | MEDICAL REMOTE CONTROLLED AUTOMATICALLY DRIVEN AFTERLOADING SYSTEMS; PARTICULAR REQUIREMENTS FOR THE SAFETY OF THE EQUIPMENT |
| DIN 6855-11:2016-08 | CONSTANCY TESTING OF NUCLEAR MEDICINE INSTRUMENTS - PART 11: RADIONUCLIDE CALIBRATORS (IEC/TR 61948-4:2006, MODIFIED) |
| DIN 57750-206 : 1984 | MEDICAL ELECTRICAL EQUIPMENT HAEMODIALYSIS EQUIPMENT - PARTICULAR REQUIREMENTS FOR SAFETY |
| DIN EN 60601-2-7 : 2000 | MEDICAL ELECTRICAL EQUIPMENT - PART 2-7: PARTICULAR REQUIREMENTS FOR THE SAFETY OF HIGH-VOLTAGE GENERATORS OF DIAGNOSTIC X-RAY GENERATORS |
| VDE 0750-2-40 : 1998 | MEDICAL ELECTRICAL EQUIPMENT - PART 2-40: PARTICULAR REQUIREMENTS FOR THE SAFETY OF ELECTROMYOGRAPHS AND EVOKED RESPONSE EQUIPMENT |
| DIN EN ISO 6875:2011-10 | DENTISTRY - PATIENT CHAIR |
| DIN EN ISO 8835-4:2009-07 | INHALATIONAL ANAESTHESIA SYSTEMS - PART 4: ANAESTHETIC VAPOUR DELIVERY DEVICES |
| DIN EN ISO 17510-2:2009-07 | SLEEP APNOEA BREATHING THERAPY - PART 2: MASKS AND APPLICATION ACCESSORIES |
| DIN EN ISO 8835-2:2009-08 | INHALATIONAL ANAESTHESIA SYSTEMS - PART 2: ANAESTHETIC BREATHING SYSTEMS |
| DIN EN ISO 18778:2009-08 | Respiratory equipment - Infant monitors - Particular requirements (ISO 18778:2005) |
| DIN EN ISO 18777:2009-07 | TRANSPORTABLE LIQUID OXYGEN SYSTEMS FOR MEDICAL USE - PARTICULAR REQUIREMENTS |
| DIN EN ISO 11608-4:2016-03 (Draft) | PEN-INJECTORS FOR MEDICAL USE - PART 4: REQUIREMENTS AND TEST METHODS FOR ELECTRONIC AND ELECTROMECHANICAL PEN-INJECTORS |
| DIN EN ISO 10650-2:2007-11 | DENTISTRY - POWERED POLYMERIZATION ACTIVATORS - PART 2: LIGHT-EMITTING DIODE (LED) LAMPS |
| DIN EN ISO 10650-1:2006-01 | DENTISTRY - POWERED POLYMERIZATION ACTIVATORS - PART 1: QUARTZ TUNGSTEN HALOGEN LAMPS |
| DIN EN ISO 10343:1999-07 | OPHTHALMIC INSTRUMENTS - OPHTHALMOMETERS (ISO 10343:2014) |
| DIN EN ISO 10651-2:2011-06 | LUNG VENTILATORS FOR MEDICAL USE - PARTICULAR REQUIREMENTS FOR BASIC SAFETY AND ESSENTIAL PERFORMANCE - PART 2: HOME CARE VENTILATORS FOR VENTILATOR-DEPENDENT PATIENTS |
| DIN EN ISO 8359:2009-08 | OXYGEN CONCENTRATORS FOR MEDICAL USE - SAFETY REQUIREMENTS |
| VDI 5702 Blatt 1:2017-04 | Medical device software - Medical SPICE Process assessment model |
| VDE 0750-2-38 : 2001 | MEDICAL ELECTRICAL EQUIPMENT - PARTICULAR REQUIREMENTS FOR THE SAFETY OF ELECTRICALLY OPERATED HOSPITALS BEDS |
| VDE 0411-2-031 : 1995 | SAFETY REQUIREMENTS FOR ELECTRICAL EQUIPMENT FOR MEASUREMENT, CONTROL AND LABORATORY USE - PARTICULAR REQUIREMENTS FOR HAND-HELD PROBE ASSEMBLIES FOR ELECTRICAL MEASUREMENT AND TEST |
| VDE 0750-2-32 : 1995 | MEDICAL ELECTRICAL EQUIPMENT - PART 2: PARTICULAR REQUIREMENTS FOR THE SAFETY OF ASSOCIATED EQUIPMENT OF X-RAY EQUIPMENT |
| VDE 0750-2-64:2018-01 | MEDICAL ELECTRICAL EQUIPMENT - PART 2-64: PARTICULAR REQUIREMENTS FOR THE BASIC SAFETY AND ESSENTIAL PERFORMANCE OF LIGHT ION BEAM MEDICAL ELECTRICAL EQUIPMENT |
| VDE 0750-2-7 : 2000 | MEDICAL ELECTRICAL EQUIPMENT - PART 2-7: PARTICULAR REQUIREMENTS FOR THE SAFETY OF HIGH-VOLTAGE GENERATORS OF DIAGNOSTIC X-RAY GENERATORS |
| DIN EN 60601-2-64:2018-01 | MEDICAL ELECTRICAL EQUIPMENT - PART 2-64: PARTICULAR REQUIREMENTS FOR THE BASIC SAFETY AND ESSENTIAL PERFORMANCE OF LIGHT ION BEAM MEDICAL ELECTRICAL EQUIPMENT |
| DIN EN ISO 81060-2:2014-10 | NON-INVASIVE SPHYGMOMANOMETERS - PART 2: CLINICAL INVASTIGATION OF AUTOMATED MEASUREMENT TYPE (ISO 81060-2:2013) |
| DIN 57753-2 : 1983 | RULES RELATING TO INTRACARDIAC APPLICATIONS OF MEDICAL ELECTRICAL EQUIPMENT |
| DIN 15990:1981-12 | DEVELOPING MACHINES FOR PHOTOGRAPHIC FILM AND PAPER (SHEET AND ROLL MATERIAL); SAFETY REGULATIONS |
| DIN EN ISO 10524-3:2013-06 | PRESSURE REGULATORS FOR USE WITH MEDICAL GASES - PART 3: PRESSURE REGULATORS INTEGRATED WITH CYLINDER VALVES (ISO 10524-3:2005 + AMD 1:2013) |
| DIN EN ISO 10651-6:2011-06 | LUNG VENTILATORS FOR MEDICAL USE - PARTICULAR REQUIREMENTS FOR BASIC SAFETY AND ESSENTIAL PERFORMANCE - PART 6: HOME-CARE VENTILATORY SUPPORT DEVICES |
| DIN EN ISO 10079-3:2014-09 | Medical suction equipment - Part 3: Suction equipment powered from a vacuum or positive pressure gas source (ISO 10079-3:2014) |
| DIN EN ISO 20072:2013-10 | AEROSOL DRUG DELIVERY DEVICE DESIGN VERIFICATION - REQUIREMENTS AND TEST METHODS (ISO 20072:2009) |
| DIN 58946-2:1982-10 | STERILIZATION - STEAM STERILIZERS - BIG STERILIZERS - REQUIREMENTS |
| DIN 6875-20:2016-08 | SPECIAL RADIOTHERAPY EQUIPMENTS - PART 20: PROTON THERAPY - RULES FOR CONSTRUCTION OF STRUCTURAL RADIATION PROTECTION |
| DIN 6868-161:2013-01 | Image quality assurance in diagnostic X-ray departments - Part 161: RoeV acceptance testing of dental radiographic equipment for digital cone-beam computed tomography |
| DIN 6818-6:1988-12 | RADIATION PROTECTION DOSIMETERS; THERMOLUMINESCENCE DOSIMETRY SYSTEMS |
| DIN VDE 0750-214 : 1992 | MEDICAL ELECTRICAL EQUIPMENT - PARTICULAR REQUIREMENTS FOR THE SAFETY OF ANAESTHETIC MACHINES |
| DIN VDE 0750-206 : 1984 | MEDICAL ELECTRICAL EQUIPMENT - HAEMODIALYSIS EQUIPMENT - PARTICULAR REQUIREMENTS FOR SAFETY |
| DIN VDE 0750-211 : 1988 | MEDICAL ELECTRICAL EQUIPMENT - MEDICAL SUPPLY UNITS - PARTICULAR REQUIREMENTS FOR SAFETY |
| DIN VDE 0753-2 : 1983 | RULES RELATING TO INTRACARDIAC APPLICATIONS OF MEDICAL ELECTRICAL EQUIPMENT |
| DIN IEC 60068-2-18:1991-04 | ELECTRICAL ENGINEERING; BASIC ENVIRONMENTAL TESTING PROCEDURES; TEST R AND GUIDANCE: WATER |
| DIN EN ISO 5359:2015-02 | ANAESTHETIC AND RESPIRATORY EQUIPMENT - LOW-PRESSURE HOSE ASSEMBLIES FOR USE WITH MEDICAL GASES (ISO 5359:2014) |
| DIN EN ISO 10650:2016-02 | DENTISTRY - POWERED POLYMERIZATION ACTIVATORS (ISO 10650:2015) |
| DIN EN ISO 8835-5:2009-07 | INHALATIONAL ANAESTHESIA SYSTEMS - PART 5: ANAESTHESIA VENTILATORS |
| DIN EN ISO 10079-1:2016-05 | MEDICAL SUCTION EQUIPMENT - PART 1: ELECTRICALLY POWERED SUCTION EQUIPMENT (ISO 10079-1:2015) |
| DIN 42801:1980-04 | CONNECTION DEVICE FOR POTENTIAL EQUALIZATION CONDUCTORS |
| DIN EN 80369-5:2017-10 | SMALL-BORE CONNECTORS FOR LIQUIDS AND GASES IN HEALTHCARE APPLICATIONS - PART 5: CONNECTORS FOR LIMB CUFF INFLATION APPLICATIONS (IEC 80369-5:2016 + COR.1:2017) |
| VDE 0753-3 : 1983 | RULES OF APPLICATION FOR CARDIAC DEFIBRILLATORS |
| VDE 0711-225 : 1995 | LUMINAIRES - PART 2: PARTICULAR REQUIREMENTS; SECTION 25: LUMINAIRES FOR USE IN CLINICAL AREAS OF HOSPITALS AND HEALTH CARE BUILDINGS |
| DIN VDE 0753-1 : 1983 | RULES OF APPLICATION FOR HIGH-FREQUENCY SURGERY |
| DIN VDE 0753-3 : 1983 | RULES OF APPLICATION FOR CARDIAC DEFIBRILLATORS |
| VDE 0750-216 : 1991 | MEDICAL ELECTRICAL EQUIPMENT - PARTICULAR REQUIREMENTS FOR THE SAFETY OF CAPACITOR DISCHARGE X-RAY GENERATORS |
| VDE 0750-222 : 1990 | MEDICAL ELECTRICAL EQUIPMENT - PARTICULAR REQUIREMENTS FOR THE SAFETY OF THERAPEUTIC X-RAY GENERATORS |
| DIN VDE 0750-216 : 1991 | MEDICAL ELECTRICAL EQUIPMENT; PARTICULAR REQUIREMENTS FOR THE SAFETY OF CAPACITOR DISCHARGE X-RAY GENERATORS |
| DIN VDE 0834 : 1991 | LUMINOUS CALL SYSTEMS - INSTALLATIONS IN HOSPITALS, NURSING HOMES AND SIMILAR INSTITUTIONS - ERECTION AND OPERATION |
| DIN EN 60601-2-32 : 1995 | MEDICAL ELECTRICAL EQUIPMENT - PART 2: PARTICULAR REQUIREMENTS FOR THE SAFETY OF ASSOCIATED EQUIPMENT OF X-RAY EQUIPMENT |
| DIN 19403:2016-08 | DENTISTRY - MULTIFUNCTION HANDPIECES |
| DIN 42801-2:1984-01 | CONNECTION DEVICE FOR POTENTIAL EQUALIZATION CONDUCTORS |
| DIN EN ISO 80601-2-69:2014-12 | Medical electrical equipment - Part 2-69: Particular requirements for basic safety and essential performance of oxygen concentrator equipment (ISO 80601-2-69:2014) |
| DIN EN ISO 10341:2013-04 | Ophthalmic instruments - Refractor heads (ISO 10341:2012) |
| DIN EN ISO 10939:2016-10 (Draft) | OPHTHALMIC INSTRUMENTS - SLIT-LAMP MICROSCOPES (ISO 10939:2017) |
| DIN EN ISO 10943:2011-11 | Ophthalmic instruments - Indirect ophthalmoscopes (ISO 10943:2011) |
| DIN EN ISO 10343:2014-10 | OPHTHALMIC INSTRUMENTS - OPHTHALMOMETERS (ISO 10343:2014) |
| DIN EN ISO 18779:2005-06 | Medical devices for conserving oxygen and oxygen mixtures - Particular requirements (ISO 18779:2005) |
| DIN EN ISO 80369-7:2017-10 | Small-bore connectors for liquids and gases in healthcare applications - Part 7: Connectors for intravascular or hypodermic applications (ISO 80369-7:2016, Corrected version 2016-12-01) |
| DIN EN ISO 8185:2009-07 | RESPIRATORY TRACT HUMIDIFIERS FOR MEDICAL USE - PARTICULAR REQUIREMENTS FOR RESPIRATORY HUMIDIFICATION SYSTEMS |
| DIN EN ISO 10939:2017-09 | OPHTHALMIC INSTRUMENTS - SLIT-LAMP MICROSCOPES (ISO 10939:2017) |
| DIN EN ISO 10079-3:2000-03 | MEDICAL SUCTION EQUIPMENT - PART 3: SUCTION EQUIPMENT POWERED FROM A VACUUM OR POSITIVE PRESSURE GAS SOURCE (ISO 10079-3:2014) |
| DIN 57753-1 : 1983 | RULES OF APPLICATION FOR HIGH-FREQUENCY SURGERY |
| DIN EN 60601-2-9 : 1999 | MEDICAL ELECTRICAL EQUIPMENT - PART 2-9: PARTICULAR REQUIREMENTS FOR THE SAFETY OF PATIENT CONTACT DOSEMETERS USED IN RADIOTHERAPY WITH ELECTRICALLY CONNECTED RADIATION DETECTORS |
| VDE 0750-214 : 1992 | MEDICAL ELECTRICAL EQUIPMENT - PARTICULAR REQUIREMENTS FOR SAFETY OF ANAESTHETIC MACHINES |
| VDE 0750-226 : 1990 | MEDICAL ELECTRICAL EQUIPMENT - DIAGNOSTIC & THERAPEUTIC LASER EQUIPMENT - PARTICULAR REQUIREMENTS FOR SAFETY |
| VDE 0750-206 : 1984 | MEDICAL ELECTRICAL EQUIPMENT - HAEMODIALYSIS EQUIPMENT - PARTICULAR REQUIREMENTS FOR SAFETY |
| VDE 0834 : 1991 | LUMINOUS CALL SYSTEMS - INSTALLATIONS IN HOSPITALS, NURSING HOMES AND SIMILAR INSTITUTIONS, ERECTION AND OPERATION |
| VDE 0753-1 : 1983 | RULES OF APPLICATION FOR HIGH-FREQUENCY SURGERY |
| VDE 0750-2-9 : 1999 | MEDICAL ELECTRICAL EQUIPMENT - PART 2-9: PARTICULAR REQUIREMENTS FOR THE SAFETY OF PATIENT CONTACT DOSEMETERS USED IN RADIOTHERAPY WITH ELECTRICALLY CONNECTED RADIATION DETECTORS |
| VDE 0753-2 : 1983 | RULES RELATING TO INTRACARDIAC APPLICATIONS OF MEDICAL ELECTRICAL EQUIPMENT |
| DIN 57753-3 : 1983 | RULES OF APPLICATION FOR CARDIAC DEFIBRILLATORS |
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