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Maxcert is offering EC Representative services for non EU medical devices manufacturers. Maxcert is authorized/ registered EC REP service provider and can manage your ECREP requirements better than others. We make sure that you are MDR ready! and well updated with the EU regulations for your medical devices. Maxcert’s team has expert knowledge to help you navigate through the complex regulatory challenges that the new EU MDR bring. We can assist you through out the entire process to ensure that you and your business are compliant with all of the EU MDR requirements. For more information, reach out to us at

We have been designing and producing UL labels for well-known industrial companies since 1990. The requirements and regulations are very complex and may require a detailed consultation in order to explain the UL-compliant marking and the different application programs. The UL certification of an end product by an OEM (Original Equipment Manufacturer) refers to every single component of the product. A label is such a component whose requirements are regulated in the UL 969 “Standard for Marking & Labeling Systems”.

teXXmo bietet maßgesschneiderte Kofferlösungen für Ihre Tablet PCs und Zubehör.

Application: Assays Product group: Reagents CAS-Nr.: [30931-67-0] Storing temperature: -20°C EINECS: 250-396-6 Synonym: 2,2'-Azino-bis-(3-ethylbenzo-thiazoline-6-sulfonic acid) diammonium salt IUPAC: 2,2'-Azino-bis(3-ethylbenzthiazoline-6-sulfonic acid) Appearance: light green powder MW: 558.69 g/mol UNSPSC-No: 41116134 Formula: C18H16N4O6S4(NH4)2 CAS Nr:[30931-67-0] Code:1362