Normy

Obsah

ČSN EN 62694 This International Standard applies to backpack-type radiation detectors (BRDs) that are used for the detection of illicit trafficking of radioactive material. This standard establishes the operational and performance requirements for BRDs. BRDs are portable instruments designed to be worn during use. They may also be used as temporary area monitors in a stand-alone mode. BRDs detect gamma radiation and may include neutron detection and/or the identification of gamma-ray emitting radionuclides. This standard establishes performance and testing requirements associated with radiation measurements and the expected electrical, mechanical, and environmental conditions while in use.

Obsah

ČSN EN 62040-5-3 This part of IEC 62040 establishes the performance and test requirements applied to movable, stationary and fixed electronic DC uninterruptible power systems (DC UPS) that are supplied from an AC voltage source not exceeding 1 000 V, deliver a DC output voltage not exceeding 1 500 V, incorporate an energy storage device, and have a primary function to ensure continuity of DC power to loads. This document specifies performance and test requirements of a complete DC UPS and not of individual DC UPS functional units. The individual DC UPS functional units are dealt with in IEC publications referred to in the bibliography that apply so far that they are not in contradiction with this document. This document does not cover conventional AC input distribution boards and their associated switches, conventional DC distribution boards and their associated switches, conventional AC UPSs covered by IEC 62040-3, low-voltage DC power supply devices covered by a specific product standard, for example IEC 61204, and those covered by a specific product standard, for example ITU communication standards, and systems wherein the output voltage is derived from a rotating machine.

Obsah

ČSN EN 15224 Tato norma specifikuje požadavky na systém managementu kvality, když organizace poskytující zdravotní péči potřebuje prokazovat svou schopnost trvale poskytovat produkty a služby, které splňují požadavky zákazníka a příslušné požadavky zákonů a předpisů, a má v úmyslu zvyšovat spokojenost zákazníka efektivním aplikováním tohoto systému, včetně procesů k jeho zlepšování, a prokazováním shody s požadavky zákazníka a s příslušnými požadavky zákonů a předpisů.

Obsah

ČSN EN ISO 19110 This document defines the methodology for cataloguing feature types. This document specifies how feature types can be organized into a feature catalogue and presented to the users of a set of geographic data. This document is applicable to creating catalogues of feature types in previously uncatalogued domains and to revising existing feature catalogues to comply with standard practice. This document applies to the cataloguing of feature types that are represented in digital form. Its principles can be extended to the cataloguing of other forms of geographic data. Feature catalogues are independent of feature concept dictionaries defined in ISO 19126 and can be specified without having to use or create a Feature Concept Dictionary. This document is applicable to the definition of geographic features at the type level. This document is not applicable to the representation of individual instances of each type. This document excludes portrayal schemas as specified in ISO 19117. This document may be used as a basis for defining the universe of discourse being modelled in a particular application, or to standardize general aspects of real world features being modelled in more than one application.

Obsah

ČSN ISO/IEC 19794-4 Tato část ISO/IEC 19794 specifikuje formát pro výměnu datových záznamů pro uchovávání, zaznamenávání a přenášení informací z jedné nebo více oblastí obrazu prstu nebo dlaně. Může být použita pro výměnu a srovnání dat obrazu prstu. Definuje obsah, formát a jednotky měření pro výměnu dat obrazu prstu, které mohou být použity v procesu registrace, ověření nebo identifikace subjektu. Informace sestává z celé škály povinných a volitelných položek, včetně skenovacích parametrů, komprimovaných nebo nekomprimovaných obrazů a informací specifických pro prodejce (dodavatele). Tyto informace jsou určeny pro výměnu mezi organizacemi, které se opírají o automatická zařízení a systémy pro účely identifikace nebo ověření založené na informacích z oblastí obrazů prstů. Informace kompilované a formátované v souladu s touto částí normy ISO/IEC 19794 mohou být zaznamenávány na strojově čitelná média nebo mohou být přenášeny zařízeními datové komunikace.

Obsah

ČSN EN ISO 7198 1.1 This International Standard specifies requirements for the evaluation of vascular prostheses and requirements with respect to nomenclature, design attributes and information supplied by the manufacturer, based upon current medical knowledge. Guidance for the development of in vitro test methods is included in an informative annex to this International Standard. This International Standard can be considered as a supplement to ISO 14630:2012, which specifies general requirements for the performance of non-active surgical implants. NOTE: Due to the variations in the design of implants covered by this International Standard and, in some cases, due to the relatively recent development of some of these implants (e.g. bioabsorbable vascular prostheses, cell based tissue engineered vascular prostheses), acceptable standardized in vitro tests and clinical results are not always available. As further scientific and clinical data become available, appropriate revision of this International Standard will be necessary. 1.2 This International Standard is applicable to sterile tubular vascular grafts implanted by direct visualization surgical techniques as opposed to fluoroscopic or other non-direct imaging (e.g. computerized tomography or magnetic resonance imaging), intended to replace, bypass, or form shunts between segments of the vascular system in humans and vascular patches intended for repair and reconstruction of the vascular system. 1.3 Vascular prostheses that are made of synthetic textile materials and synthetic non-textile materials are within the scope of this International Standard. 1.4 While vascular prostheses that are made wholly or partly of materials of non-viable biological origin, including tissue engineered vascular prostheses are within the scope, this International Standard does not address sourcing, harvesting, manufacturing and all testing requirements for biological materials. It is further noted that different regulatory requirements might exist for tissues from human and animal sources. 1.5 Compound, coated, composite, and externally reinforced vascular prostheses are within the scope of this standard. 1.6 Endovascular prostheses implanted using catheter delivery and non-direct visualization are excluded from the scope of this International Standard. This International Standard includes information on the development of appropriate test methods for graft materials, referenced in ISO 25539-1 for materials used in the construction of endovascular prostheses (i.e. stent-grafts). NOTE: Requirements for endovascular prostheses are specified in ISO 25539-1. 1.7 The valve component of valved conduits constructed with a tubular vascular graft component, and the combination of the valved component and the tubular vascular graft component, are excluded from the scope of this International Standard. This International Standard can be helpful in identifying the appropriate evaluation of the tubular vascular graft component of a valved conduit but specific requirements and testing are not described for these devices. 1.8 Cardiac and pericardial patches, vascular stents, accessory devices such as anastomotic devices, staplers, tunnelers and sutures, and pledgets are excluded from the scope of this International Standard. NOTE: Requirements for vascular stents are specified in ISO 25539-2. 1.9 Requirements regarding cell seeding are excluded from the scope of this International Standard. Tissue engineered vascular prostheses that contain or are manufactured using cells present many distinct manufacturing (e.g. aseptic processing, cell seeding, etc.) and testing issues than those produced with synthetic or non-viable biological materials. The in vitro testing requirements that are outlined in this International Standard can be a useful guide for certain testing requirements for these cell-based products. 1.10 Pharmacological aspects of drug-eluting or drug-coated vascular prostheses are not addressed in this International Standard. NOTE: Requirements for vascular device-drug combination products are specified in ISO 12417-1. 1.11 Degradation, tissue ingrowth and/or tissue replacement, and other time-dependent aspects of absorbable vascular prostheses are not addressed in the standard.

Obsah

ČSN ETSI EN 300 220-1 V3.1.1 The present document specifies technical characteristics and test methods to be used in the conformance assessment of Short Range Device equipment in the frequency range 25 MHz to 1 GHz.

Obsah

ČSN ETSI EN 300 330 V2.1.1 The present document specifies technical characteristics and methods of measurements for the following Short Range Device major equipment types: 1) Generic Short range Devices including transmitters and receivers operating in the range from 9 kHz to 25 MHz; and 2) inductive loop transmitters and receivers operating from 9 kHz to 30 MHz including Radio Frequency Identification (RFID), Near Field Communication (NFC) and Electronic Article Surveillance (EAS) operating in LF and HF ranges. Also the present document covers fixed, mobile and portable stations. NOTE: If a system includes transponders, these are measured together with the transmitter. The frequency ranges and limits of the present document are based on the European Commission Decision for SRDs [i.10], CEPT/ERC/REC 70-03 [i.1]. When selecting parameters for new SRDs, which may have inherent safety of human life implications, manufacturers and users should pay particular attention to the potential for interference from other systems operating in the same or adjacent bands. The radio equipment, covered by the present document is divided into several classes which are dependent on the antenna used (see annex B). Three types of measuring methods are defined in the present document due to the varied nature of the antenna types for equipment used in this band. One method measures the RF carrier current, another measures the radiated H-field and the third conducted power. The present document covers the essential requirements of article 3.2 of Directive 2014/53/EU [i.4] under the conditions identified in annex A.

Obsah

ČSN EN 378-2 Platí úvod uvedený v EN 378-1. Tato norma je norma typu C, jak je stanoveno v EN ISO 12100. Příslušná strojní zařízení a rozsah zahrnutých nebezpečí, nebezpečných situací a událostí je uveden v předmětu této normy. Pro stroje, které byly konstruovány a vyrobeny podle ustanovení této normy typu C platí, že pokud se ustanovení této normy typu C odlišují od ustanovení, která jsou stanovena v normách typu A nebo B, mají ustanovení této normy typu C přednost před ustanoveními jiných norem.

Obsah

ČSN EN 61987-11 ed. 2 This part of IEC 61987 provides: a characterisation of industrial process measuring equipment (device type dictionary) for integration in the Common Data Dictionary (CDD), and generic structures for operating lists of properties (OLOP) and device lists of properties (DLOP) of measuring equipment in conformance with IEC 61987-10. The generic structures for the OLOP and DLOP contain the most important blocks for process measuring equipment. Blocks pertaining to a specific equipment type will be described in the corresponding part of the IEC 61987 standard series. Similarly, equipment properties are not part of IEC 61987-11. For in-stance, the OLOP and DLOP for flow transmitters with blocks and properties are to be found in IEC 61987-12.

Obsah

ČSN EN 55016-1-5 ed. 2 Tato část souboru norem určuje požadavky na stanoviště pro kalibraci v kmitočtovém rozsahu 5 MHz až 18 GHz, která se použijí pro provedení kalibrace antény podle ČSN EN 55016-1-6 (33 4210). Také určuje požadavky na referenční zkušební stanoviště (REFTS), které se používají pro validaci zkušebních stanovišť pro vyhovění (COMTS) v kmitočtovém rozsahu 30 MHz až 1 000 MHz podle ČSN EN 55016-1-4 ed. 3 (33 4210). Tato část souboru norem má status základní normy EMC. Měřicí vybavení je uvedeno v ČSN EN 55016-1-1 ed. 3 (33 4210) a v ČSN EN 55016-1-4 ed. 3 (33 4210). Další informace a základy o nejistotách obecně jsou uvedeny v CISPR 16-4, který také může napomoci při odhadu nejistoty pro kalibrační postupy antén a měření při validaci stanoviště.

Obsah

ČSN ISO 3767-1 Tento dokument normalizuje značky pro použití na ovládačích obsluhy a jiných sdělovačích použitelných v rozmanitých typech zemědělských traktorů a strojů, lesnických strojů a motorových žacích a zahradních strojů. POZNÁMKA 1: ISO 3767-2 zahrnuje značky pro zemědělské traktory a stroje. ISO 3767-3 zahrnuje značky pro žací a zahradní stroje. ISO 3767-4 zahrnuje značky pro lesnické stroje. ISO 3767-5 zahrnuje značky pro ruční přenosné lesnické stroje. POZNÁMKA 2: ISO 7000 a IEC 60417 mohou být nápomocny pro další mezinárodně normalizované značky s možným vztahem k zemědělským traktorům a strojům, lesnickým strojům a motorovým žacím a zahradním strojům.