|
DIN ISO 7000:2008-12
|
Graphical symbols for use on equipment - Index and synopsis (ISO 7000:2004 + ISO 7000 Database:2008 up to ISO 7000-2750)
|
|
ISO 7010:2011
|
Graphical symbols Safety colours and safety signs Registered safety signs
|
|
DIN EN ISO 14644-1:2016-06
|
CLEANROOMS AND ASSOCIATED CONTROLLED ENVIRONMENTS - PART 1: CLASSIFICATION OF AIR CLEANLINESS BY PARTICLE CONCENTRATION (ISO 14644-1:2015)
|
|
DIN EN ISO 15223-1:2015-08 (Draft)
|
MEDICAL DEVICES - SYMBOLS TO BE USED WITH MEDICAL DEVICE LABELS, LABELLING AND INFORMATION TO BE SUPPLIED - PART 1: GENERAL REQUIREMENTS (ISO 15223-1:2016, CORRECTED VERSION 2017-03)
|
|
ISO 80601-2-67:2014
|
Medical electrical equipment Part 2-67: Particular requirements for basic safety and essential performance of oxygen-conserving equipment
|
|
ISO 3744:2010
|
Acoustics Determination of sound power levels and sound energy levels of noise sources using sound pressure Engineering methods for an essentially free field over a reflecting plane
|
|
DIN EN ISO 7396-1:2016-09
|
MEDICAL GAS PIPELINE SYSTEMS - PART 1: PIPELINE SYSTEMS FOR COMPRESSED MEDICAL GASES AND VACUUM (ISO 7396-1:2016)
|
|
EN 15986:2011
|
Symbol for use in the labelling of medical devices - Requirements for labelling of medical devices containing phthalates
|
|
DIN EN ISO 80601-2-67:2012-02 (Draft)
|
MEDICAL ELECTRICAL EQUIPMENT - PART 2-67: PARTICULAR REQUIREMENTS FOR BASIC SAFETY AND ESSENTIAL PERFORMANCE OF OXYGEN CONSERVING EQUIPMENT (ISO/DIS 80601-2-67:2012)
|
|
IEC 60601-1:2005+AMD1:2012 CSV
|
Medical electrical equipment - Part 1: General requirements for basic safety and essential performance
|
|
CFR 45(PTS1-199) : OCT 2017
|
PUBLIC WELFARE - SUBTITLE A - DEPARTMENT OF HEALTH AND HUMAN SERVICES - GENERAL ADMINISTRATION - SUBTITLE B - REGULATIONS RELATING TO PUBLIC WELFARE
|
|
DIN EN 60601-1-6 : 2016
|
MEDICAL ELECTRICAL EQUIPMENT - PART 1-6: GENERAL REQUIREMENTS FOR BASIC SAFETY AND ESSENTIAL PERFORMANCE - COLLATERAL STANDARD: USABILITY (IEC 60601-1-6:2010 + A1:2013)
|
|
VDE 0750-1-2 : 2016
|
MEDICAL ELECTRICAL EQUIPMENT - PART 1-2: GENERAL REQUIREMENTS FOR BASIC SAFETY AND ESSENTIAL PERFORMANCE - COLLATERAL STANDARD: ELECTROMAGNETIC DISTURBANCES REQUIREMENTS AND TESTS (IEC 60601-1-2:2014)
|
|
IEC 60601-1-6:2010+AMD1:2013 CSV
|
Medical electrical equipment - Part 1-6: General requirements for basic safety and essential performance - Collateral standard: Usability
|
|
DIN EN ISO 17664:2016-06 (Draft)
|
PROCESSING OF HEALTH CARE PRODUCTS - INFORMATION TO BE PROVIDED BY THE MEDICAL DEVICE MANUFACTURER FOR THE PROCESSING OF MEDICAL DEVICES (ISO 17664:2017)
|
|
DIN EN 62366 : 2016
|
MEDICAL DEVICES - APPLICATION OF USABILITY ENGINEERING TO MEDICAL DEVICES (IEC 62366:2007 + A1:2014)
|
|
ISO 14937:2009
|
Sterilization of health care products General requirements for characterization of a sterilizing agent and the development, validation and routine control of a sterilization process for medical devices
|
|
ISO 8835-7:2011
|
Inhalational anaesthesia systems — Part 7: Anaesthetic systems for use in areas with limited logistical supplies of electricity and anaesthetic gases
|
|
DIN EN ISO 14971:2013-04
|
MEDICAL DEVICES - APPLICATION OF RISK MANAGEMENT TO MEDICAL DEVICES (ISO 14971:2007)
|
|
ISO 10083:2006
|
Oxygen concentrator supply systems for use with medical gas pipeline systems
|
|
VDE 0750-1-6 : 2016
|
MEDICAL ELECTRICAL EQUIPMENT - PART 1-6: GENERAL REQUIREMENTS FOR BASIC SAFETY AND ESSENTIAL PERFORMANCE - COLLATERAL STANDARD: USABILITY (IEC 60601-1-6:2010 + A1:2013)
|
|
DIN EN ISO 3744:2011-02
|
Acoustics - Determination of sound power levels and sound energy levels of noise sources using sound pressure - Engineering methods for an essentially free field over a reflecting plane (ISO 3744:2010)
|
|
IEC 60601-1-8:2006+AMD1:2012 CSV
|
Medical electrical equipment - Part 1-8: General requirements forbasic safety and essential performance - Collateral Standard: General requirements, tests and guidance for alarm systems inmedical electrical equipment and medical electrical systems
|
|
IEC 62366:2007+AMD1:2014 CSV
|
Medical devices - Application of usability engineering to medical devices
|
|
IEC 60601-1-2:2014
|
Medical electrical equipment - Part 1-2: General requirements for basic safety and essential performance - Collateral Standard: Electromagnetic disturbances - Requirements and tests
|
|
DIN ISO 10083:2008-12
|
OXYGEN CONCENTRATOR SUPPLY SYSTEMS FOR USE WITH MEDICAL GAS PIPELINE SYSTEMS
|
|
ISO 8185:2007
|
Respiratory tract humidifiers for medical use Particular requirements for respiratory humidification systems
|
|
ISO/TR 16142:2006
|
Medical devices Guidance on the selection of standards in support of recognized essential principles of safety and performance of medical devices
|
|
ISO 14159:2002
|
Safety of machinery — Hygiene requirements for the design of machinery
|
|
ISO 80369-1:2010
|
Small-bore connectors for liquids and gases in healthcare applications Part 1: General 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 ISO 14159:2008-07
|
SAFETY OF MACHINERY - HYGIENE REQUIREMENTS FOR THE DESIGN OF MACHINERY
|
|
DIN EN ISO 80369-1:2015-09 (Draft)
|
SMALL BORE CONNECTORS FOR LIQUIDS AND GASES IN HEALTHCARE APPLICATIONS - PART 1: GENERAL REQUIREMENTS
|
|
ISO 14971:2007
|
Medical devices Application of risk management to medical devices
|
|
ISO 7000:2014
|
Graphical symbols for use on equipment Registered symbols
|
|
ISO 4135:2001
|
Anaesthetic and respiratory equipment Vocabulary
|
|
DIN EN ISO 7010:2012-10
|
GRAPHISCHE SYMBOLE - SICHERHEITSFARBEN UND SICHERHEITSZEICHEN - REGISTRIERTE SICHERHEITSZEICHEN (ISO 7010:2011/AMD 5:2014)
|
|
ISO 10524-1:2006
|
Pressure regulators for use with medical gases Part 1: Pressure regulators and pressure regulators with flow-metering devices
|
|
ISO 15223-1:2016
|
Medical devices Symbols to be used with medical device labels, labelling and information to be supplied Part 1: General requirements
|
|
VDE 0750-1 : 2013
|
MEDICAL ELECTRICAL EQUIPMENT - PART 1: GENERAL REQUIREMENTS FOR BASIC SAFETY AND ESSENTIAL PERFORMANCE (IEC 60601-1:2005 + COR.:2006 + COR.:2007 + A1:2012)
|
|
VDE 0750-1-11 : 2016
|
MEDICAL ELECTRICAL EQUIPMENT - PART 1-11: GENERAL REQUIREMENTS FOR BASIC SAFETY AND ESSENTIAL PERFORMANCE - COLLATERAL STANDARD: REQUIREMENTS FOR MEDICAL ELECTRICAL EQUIPMENT AND MEDICAL ELECTRICAL SYSTEMS USED IN THE HOME HEALTHCARE ENVIRONMENT (IEC 60601-1-11:2015)
|
|
ISO 17664:2017
|
Processing of health care products Information to be provided by the medical device manufacturer for the processing of medical devices
|
|
DIN EN ISO 4135:2002-03
|
Anaesthetic and respiratory equipment - Vocabulary (ISO 4135:2001); Trilingual version EN ISO 4135:2001
|
|
DIN EN 60601-1-11 : 2016
|
MEDICAL ELECTRICAL EQUIPMENT - PART 1-11: GENERAL REQUIREMENTS FOR BASIC SAFETY AND ESSENTIAL PERFORMANCE - COLLATERAL STANDARD: REQUIREMENTS FOR MEDICAL ELECTRICAL EQUIPMENT AND MEDICAL ELECTRICAL SYSTEMS USED IN THE HOME HEALTHCARE ENVIRONMENT (IEC 60601-1-11:2015)
|
|
ISO 7396-1:2016
|
Medical gas pipeline systems — Part 1: Pipeline systems for compressed medical gases and vacuum
|
Important note : All end users must be registered with an Account prior to user licenses being assigned.