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Universal Manual Operating Table REXMED ROT-160X

Model No.
ROT-160X
Made in
Taiwan
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    Universal Operating Table ROT-160X

    Key Features

    MOD. ROT-160X, Universal Manual Operating Table, HS CODE: 940290, UNCCS CODE: 381590, UNSPSC CODE: 42295112, UMDNS CODE: 13961, GMDN CODE: 36867, Main construction: Cast aluminium, powder coated steel and SS304, Table top: 5 sections table top L200xW50cm, Table rotation: 360°, Slide stroke: No, Table elevation: 74~104cm, Kidney elevation: 0~12cm, 15° Left/Right tilt with 4cm mattress, Reverse trendelenburg/Trendelenburg: 30° / 25°, Lateral tilt (Left/Right): 25° / 25°, Flex/Reflex: 80° / No, Head section: Vertical -90~30° (L25xW32cm), Arm rest: Horizontal 0~180° (L50xW13cm x 2pcs), Back section: Vertical 0~80° (L61xW50cm), Seat section: Vertical -25~30° (L50xW50cm), Leg section: Vertical -90°~20°, horizontal split leg section 0~180° (L55xW24cm x 2pcs), Perineal cut-out: Yes, Side rail: SS304 W0.8xH3cm, Base: Rectangular base with SS304 cover, 4 castors and central locking device, Control: Manual control for head, back and leg section, with one crank handle at the head end of table to control reverse trendelenburg/trendelenburg and lateral tilt, with one crank handle at the head end of table to control kidney elevator and foot operated hydraulic height adjustment, Controller voltage: No, AC/DC function: No, UPS: No, Max. patient weight: 250 KGS, W/S: anaesthetic screen frame with a square clamp x 1set, head section x 1pc, adjustable shoulder support with a square clamp x 1pair, arm rest x 1pair, adjustable body support with a square clamp x 1pair, leg crutch with a multi direction clamp x 1pair, leg section x 1pair, 4cm antistatic mattresses x 1set, O ring x 2pcs, X-ray translucent top x 1set

    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.
    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.
    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.
    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.
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