We distribute our products exclusively via the specialized trade. Therefore, we would be glad to give you the name of a local distributor. Contact us.
The CE marking is placed on medical products that are subject to the current European directives. The producer confirms by the CE mark on the product that the marketed product meets the requirements of the directive 93/42/EEC about medical devices or directive 98/79/EC about in-vitro diagnostics and the legal requirements are complied with. A written conformity declaration is being provided, which certifies the accordance with the declared directives and standards.
The term In-vitro diagnostics (IVD) refers to medical products that are being used for in-vitro examinations of samples taken from the human body, including blood and tissue donations, and exclusively or mainly serve to give information
– about physiological or pathological conditions
– about congenital anomalies or for
– for harmlessness and tolerance test with the potential recipients
– for monitoring therapeutic measures
The Medical Devices Act regulates the placing on the market and operating of medical devices. Since 1998, the CE marking is required for every medical device, since 2003 for every IVD product. Medical devices without CE marking must not be sold or operated / used within the European Union.
Please consider the “Sales unit” mentioned under “Specifications” of each product as minimum order quantity.
Of course, you can contact us in the case of damage or the like. Please ensure that the instruments are clean, residue-free or sterilized properly.
For more information see our service page.
Authorized Economic Operator – certificate number AEOC 111503
Microslides are made of a glass type that is subject to a natural aging process.
This has a negative effect on the quality. Please take note of the storage guidelines
that are printed on each box containing 5000 pieces.
The letters stand for the accuracy classes:
– class A for higher accuracy
– class AS for higher accuracy of burettes and pipettes with definded waiting time
– class B for lower accuracy
The German Measurement and Calibration Regulation – valid from January 1, 2015 – requires certification of conformity by the manufacturer for volumetric instruments used for medical, pharmaceutical and commercial measurements (e.g. manufacture and testing of drugs). The regulatory compliance is certified by the marking DE-M. The conformity guarantees the compliance of the instrument with the German Measurement and Calibration Regulation and the valid standards.
For details of the procedure, please refer to the German Measurement and Calibration Regulation.
The user is responsible for application and providing of conformity certified instruments. The certificate of conformity is valid indefinitely unless otherwise specified by the manufacturer. Conformity certified instruments that have been manufactured before 1 January 2015, may still be used. Hecht certifies the conformity of volumetric instruments directly on the instrument. In case of disposable micropipettes on the inner packing. For some liquid handling instruments in the directions for use accompanying the instrument.
A lot certificate (showing mean value of production lot) is included in each original packing. An individual certificate of performance (showing the actually determined volume of the instrument) is available on request. Please specify in your order!