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This test method is based on ISO 16000-23 and is adjusted for the measurement of indoor-light-active photocatalytic materials
and the corresponding test methods for reusable syringes having a graduated capacity from 1 to 100 ml
BS EN 61788-14 provides you with terms
requirements and tests to ensure interchangeability between plug-in type bushings and separable connectors
In vitro diagnostic medical Devices. Information supplied by the manufacturer (labelling) - In vitro diagnostic reagents for self-testing algolia-ignore This test method is based1 Scope This part of ISO 18113 specifies requirements for information supplied by the manufacturer of IVD reagents for self testing. This part of ISO 18113 also applies to information supplied by the manufacturer with calibrators and control materials intended for use with IVD medical devices for self testing. This part of ISO 18113 can also be applied to accessories. This part of ISO 18113 applies to the labels for outer and immediate containers and