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00019670
Petroleum and related products - Alternative fuels and fuel blending components assessment guide - Information to producers and blenders of automotive fuels
DIN CEN ISO/TS 17664-3
Processing of health care products - Information to be provided by the medical device manufacturer for the processing of medical devices - Part 3: Guidance on the designation of a reusable medical device to a quantitative cleaning classification
DIN CEN/T? 00019670
Petroleum and related products - Alternative fuels and fuel blending components assessment guide - Information to producers and blenders of automotive fuels
DIN EN IEC 62635
Guidelines for end-of-life information provided by manufacturers and recyclers and for recyclability rate calculation of electrical and electronic equipment
DIN EN ISO 15223-1/ A1
Medical devices - Symbols to be used with information to be supplied by the manufacturer - Part 1: General requirements - Amendment 1 (ISO 15223-1:2021/DAM 1:2024); German and English version EN ISO 15223-1:2021/prA1:2024
DIN EN ISO 20417
Medical devices - Information to be supplied by the manufacturer (ISO/DIS 20417:2024); German and English version prEN ISO 20417:2024
DIN EN ISO 29001/A1
Petroleum, petrochemical and natural gas industries - Sector-specific quality management systems - Requirements for product and service supply organizations - Amendment 1: Climate action changes (ISO 29001:2020/Amd 1:2024); English version EN ISO 29001:2020/A1:2024
DIN ISO 22931
Measurement of radioactivity in the environment - Air: Radon-222 - Quality assurance and quality control for calibration facilities, radon measurement device manufacturers and measurement device analysis providers
EN ISO 15223-1/prA1
Medical devices - Symbols to be used with information to be supplied by the manufacturer - Part 1: General requirements - Amendment 1: Addition of defined term for authorized representative and Modified EC REP symbol to not be country or region specific (ISO 15223 1:2021/DAM 1:2024)
ISO 15223-1 DAM 1
Medical devices - Symbols to be used with information to be supplied by the manufacturer - Part 1: General requirements - Amendment 1: Addition of defined term for authorized representative and Modified EC REP symbol to not be country or region specific