HomeProductsHospital BedManual Control ICU Hospital Bed REXMED RHB-100M
LEFT MENU
Enlarge

Manual Control ICU Hospital Bed REXMED RHB-100M

Model No.
RHB-100M
Made in
Taiwan
Request for Quotation
Contact Supplier

    ICU Hospital Bed RHB-100M

    Key Features

    MOD. RHB-100M, Manual Control ICU Hospital Bed, HS CODE: 940290, UNCCS CODE: 381520, UNSPSC CODE: 42191800, UMDNS CODE: 10353, GMDN CODE: 34871, Main construction: Powder coated steel, SS304 and ABS, Table top: 4 sections table top L217xW96cm, side rail up: 107cm, side rail open: 131cm, Side rail down: 96cm, Table top surface: Removable ABS plastic table top L194xW92.5cm, Table rotation: 360° manually, Mattress base: L194xW92.5cm with 6 anti-slip stopper and 8 holes for body strap, Bed height without mattress: 45~75 cm adjustable by Hi-Lo crank, Side rail: L76.5xW31.5cm x 4pcs foldable side rail, Head/Foot board: L93xW41.5cm x 2pcs removable board, Back section: 0~75° adjustable by BACK crank (L68xW93cm), Bottom section: L17.5xW93cm, Thigh section: 0~40° adjustable by KNEE crank (L29.5xW93cm), Leg section: -15~22° adjustable manually (L67.5xW93cm), Reverse trendelenburg/Trendelenburg: No / No, Bumpers: 4 bumpers at 4 corners, IV poles: 1 x adjustable height IV pole (IV pole holes for 6 places), Hanger for drainage bag: 2 on each side, Push handle for easy transport: Yes, on the head and foot board, Base: Powder coated steel base with 5" dust proof lockable castors x 4pcs, Control: Manual control with 3 x hydraulic stick for BACK, HI-LO and KNEE adjustment, Controller voltage: No, AC/DC function: No, UPS: No, Max. patient weight: 230 KGS, W/S: two section IV pole (adjustable height 85~150 cm) x 1pc, High density PU foam mattress (L190xW90xH10cm) x 1pc

    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.
    Other Products

    You may also like