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Tabletop Centrifuge REXMED RCT-130+A1504

Model No.
RCT-130+A1504
Made in
Taiwan
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    Key Features

    MOD. RCT-130+A1504, AC 110/230V, Plug type: , Tabletop centrifuge, HS CODE: 993199, UNCCS CODE: 484180, UMDNS CODE: 10780, Main construction: ABS and base with 3 suction rubber feet, Motor: Noiseless powerful brushless induction motor, Speed: 300~3,200rpm adjustable, Speed display: no, Max. R.C.F (G-force): 1,100, Timer: 0~30min adjustable mechanical timer, Short run key: No, Brake: No, Rotor type: 45°, Number of tubes: 4pcs, Centrifuge tube size: 0.5~15ml, Tube holder size: 10~15ml (17.5X98mm) x 4pcs, Lid interlock: no, Safety device: Power OFF when lid is open, auto balance system, ventilation system, fuse, bell at the end of operation, W/S: Rotor A1504 X 1pc, 10~15ml (17.5X98mm) x 4pcs

    Product Certification

    CE Marking (EU Standards) The safety mark is a mandatory conformity mark on designated products placed on the single market in the European Union (EU). This mark is possible to be affixed to only the products that conform to the safety regulation, that the directives from the ministerial conference of the European Communities show.
    The ISO 9000 family addresses various aspects of quality management and contains some of ISO’s best known standards. The standards provide guidance and tools for companies and organizations who want to ensure that their products and services consistently meet customer’s requirements, and that quality is consistently improved.
    ISO 13485:2016 specifies requirements for a quality management system where an organization needs to demonstrate its ability to provide medical devices and related services that consistently meet customer and applicable regulatory requirements. Such organizations can be involved in one or more stages of the life-cycle, including design and development, production, storage and distribution, installation, or servicing of a medical device and design and development or provision of associated activities (e.g. technical support). ISO 13485:2016 can also be used by suppliers or external parties that provide product, including quality management system-related services to such organizations.
    GMP refers to the Good Manufacturing Practice Regulations promulgated by the US Food and Drug Administration under the authority of the Federal Food, Drug, and Cosmetic Act (See Chapter IV for food, and Chapter V, Subchapters A, B, C, D, and E for drugs and devices.) These regulations, which have the force of law, require that manufacturers, processors, and packagers of drugs, medical devices, some food, and blood take proactive steps to ensure that their products are safe, pure, and effective. GMP regulations require a quality approach to manufacturing, enabling companies to minimize or eliminate instances of contamination, mixups, and errors. This in turn, protects the consumer from purchasing a product which is not effective or even dangerous. Failure of firms to comply with GMP regulations can result in very serious consequences including recall, seizure, fines, and jail time. GMP regulations address issues including recordkeeping, personnel qualifications, sanitation, cleanliness, equipment verification, process validation, and complaint handling. Most GMP requirements are very general and open-ended, allowing each manufacturer to decide individually how to best implement the necessary controls. This provides much flexibility, but also requires that the manufacturer interpret the requirements in a manner which makes sense for each individual business. GMP is also sometimes referred to as "cGMP". The "c" stands for "current," reminding manufacturers that they must employ technologies and systems which are up-to-date in order to comply with the regulation. Systems and equipment used to prevent contamination, mixups, and errors, which may have been "top-of-the-line" 20 years ago, may be less than adequate by today's standards.

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