发布日期：2013-07-01 实施日期：2013-07-01
In-vitro-Diagnostika. Messung von Groessen in Proben biologischen Ursprungs. Metrologische Rueckfuehrbarkeit von Werten,die Kalibriermaterialien und Kontrollmaterialien zugeordnet sind In vitro diagnos...
适用范围：ISO 17511:2003 specifies how to assure the metrological traceability of values assigned to calibrators and control materials intended to establish or verify trueness of measurement. The calibrators and...
实施日期：2003-08-19
Biological evaluation of medical devices. Tests for irritation and skin sensitization
适用范围：This part of ISO 10993 describes the procedure for the assessment of medical devices and their constituentmaterials with regard to their potential to produce irritation and skin sensitization.This part...
发布日期：2010-10-31
In vitro diagnostic test systems. Requirements for blood-glucosemonitoring systems for self-testing in managing diabetes mellitus
发布日期：2013-06-30 实施日期：2013-06-30
In vitro diagnostic medical devices. Measurement of quantities in samples of biological origin. Requirements for content and presentation of reference measurement procedures second edition
发布日期：2009-04-28 实施日期：2009-05-01
In vitro diagnostic medical devices. Information supplied by the manufacturer with in vitro diagnostic reagents for staining in biology
发布日期：2013-03-31 实施日期：2013-03-31
In vitro diagnostic medical devices. Information supplied by the manufacturer (labelling). Part 5:In vitro diagnostic instruments for self-testing first edition
发布日期：2009-12-09 实施日期：2009-12-15
In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 4: In vitro diagnostic reagents for self-testing
适用范围：This part of DIN EN ISO 18113 specifies requirements for information supplied by the manufacturer of IVD reagents for self-testing. Furthermore, this part of DIN EN ISO 18113 applies to information sup...
实施日期：2010-05-01
Foodstuffs - Methods of analysis for the detection of genetically modified organisms and derived products - General requirements and definitions (ISO 24276:2006 + Amd 1:2013); German version EN ISO 242...
In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 5: In vitro diagnostic instruments for self-testing
适用范围：This part of DIN EN ISO 18113 specifies requirements for information supplied by the manufacturer of IVD reagents for self-testing. Furthermore, this part of DIN EN ISO 18113 applies to information sup...
实施日期：2010-05-01
Determination of sunscreen UVA photoprotection in vitro
适用范围：ISO 24443:2012 specifies an in vitro procedure to characterize the UVA protection of sunscreen products. Specifications are given to enable determination of the spectral absorbance characteristics of U...
发布日期：2012-06-01 实施日期：2012-06-01
In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 2: In vitro diagnostic reagents for professional use
适用范围：This part of DIN EN ISO 18113 specifies requirements for information supplied by the manufacturer of IVD reagents for professional use. Furthermore, this part of DIN EN ISO 18113 also applies to inform...
实施日期：2010-05-01
实施日期：2009-12-01
In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 3: In vitro diagnostic instruments for professional use
适用范围：This part of DIN EN ISO 18113 specifies requirements for information supplied by the manufacturer of IVD instruments for professional use. Furthermore, this part of DIN EN ISO 18113 also applies to app...
实施日期：2010-05-01
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