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| 341 |
ISO 80601-2-67:2014
Medical electrical equipment -- Part 2-67: Particular requirements for basic safety and essential performance of oxygen-conserving equipment |
| 342 |
ISO 80601-2-69:2014
Medical electrical equipment -- Part 2-69: Particular requirements for basic safety and essential performance of oxygen concentrator equipment |
| 343 |
BS 8601:2013Specification for subsoil and requirements for use Specification for subsoil and requirements for use |
| 344 |
BS EN 60601-2-65 / A2:2013Medical electrical equipment Part 2-65: Particular requirements for the basic safety and essential performance of dental intra-oral X-ray equipment Medical electrical equipment Part 2-65: Particular requirements for the basic safety and essential performance of dental intra-oral X-ray equipment |
| 345 |
DIN CEN/TS 16010:2013Plastics - Recycled plastics - Sampling procedures for testing plastics waste and recyclates; German version CEN/TS 16010:2013 Plastics - Recycled plastics - Sampling procedures for testing plastics waste and recyclates; German version CEN/TS 16010:2013 |
| 346 |
DIN CEN/TS 16011:2013Plastics - Recycled plastics - Sample preparation; German version CEN/TS 16011:2013 Plastics - Recycled plastics - Sample preparation; German version CEN/TS 16011:2013 |
| 347 |
EN 60127-7:2013Miniature fuses - Part 7: Miniature fuse-links for special applicationsIEC 60127-7:2013 Miniature fuses - Part 7: Miniature fuse-links for special applicationsIEC 60127-7:2013 |
| 348 |
EN 60143-2:2013Series capacitors for power systems - Part 2: Protective equipment for series capacitor banksIEC 60143-2:2012 Series capacitors for power systems - Part 2: Protective equipment for series capacitor banksIEC 60143-2:2012 |
| 349 |
IEC 60191-4:2013
Mechanical standardization of semiconductor devices - Part 4: Coding system and classification into forms of package outlines for semiconductor device packages |
| 350 |
IEC 60601-1-10:2007/AMD1:2013
Amendment 1 - Medical electrical equipment - Part 1-10: General requirements for basic safety and essential performance - Collateral Standard: Requirements for the development of physiologic closed-loop controllers |
| 351 |
IEC 60601-1-10:2007+AMD1:2013 CSV
Medical electrical equipment - Part 1-10: General requirements forbasic safety and essential performance - Collateral Standard: Requirements for the development of physiologic closed-loopcontrollers |
| 352 |
IEC 60601-1-3:2008/AMD1:2013
Amendment 1 - Medical electrical equipment - Part 1-3: General requirements for basic safety and essential performance - Collateral Standard: Radiation protection in diagnostic X-ray equipment |
| 353 |
IEC 60601-1-3:2008+AMD1:2013 CSV
Medical electrical equipment - Part 1-3: General requirements forbasic safety and essential performance - Collateral Standard: Radiation protection in diagnostic X-ray equipment |
| 354 |
IEC 60601-1-6:2010/AMD1:2013
Amendment 1 - Medical electrical equipment - Part 1-6: General requirements for basic safety and essential performance - Collateral standard: Usability |
| 355 |
IEC 60601-1-6:2010+AMD1:2013 CSV
Medical electrical equipment - Part 1-6: General requirements forbasic safety and essential performance - Collateral standard: Usability |
| 356 |
IEC 60601-1-9:2007/AMD1:2013
Amendment 1 - Medical electrical equipment - Part 1-9: General requirements for basic safety and essential performance - Collateral Standard: Requirements for environmentally conscious design |
| 357 |
IEC 60601-1-9:2007+AMD1:2013 CSV
Medical electrical equipment - Part 1-9: General requirements forbasic safety and essential performance - Collateral Standard: Requirements for environmentally conscious design |
| 358 |
IEC 60601-2-11:2013
Medical electrical equipment - Part 2-11: Particular requirements for the basic safety and essential performance of gamma beam therapy equipment |
| 359 |
IEC 60601-2-17:2013
Medical electrical equipment - Part 2-17: Particular requirements for the basic safety and essential performance of automatically-controlled brachytherapy afterloading equipment |
| 360 |
IEC 60601-2-33:2010/AMD1:2013
Amendment 1 - Medical electrical equipment - Part 2-33: Particular requirements for the basic safety and essential performance of magnetic resonance equipment for medical diagnosis |




