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Bicakcilar-Medical Disposable Catalog 12th Edition
98Pages

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Catalog excerpts

Bicakcilar-Medical Disposable Catalog 12th Edition - 1

Touching Lives One Device at a Time Medical Disposable L Solutions ' .TTsTiT^'' : 12th Edition All products and product specifications identified in the product catalogue are based upon the information available to Bicakcilar at the time of publication. Bicakcilar reserves the right to discontinue any of these products or to change any such specifications without prior notice.

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Bicakcilar-Medical Disposable Catalog 12th Edition - 3

YEARS OF EXPERIENCE Bicakcilar is the leading disposable medical device and electro-medical device manufacturer in Turkey. The company was founded in 1959. Through the years, Bicakcilar brand has gained wide acceptance and has established a tradition of sustained reliability and customer satisfaction. As Bicakcilar employees, together with our business partners, we serve our customers by manufacturing and supplying innovative, reliable and environment friendly medical devices. We diligently value our brand and its benefit to society. Mission Our compassion for healthy life is leading us to...

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Bicakcilar-Medical Disposable Catalog 12th Edition - 5

31.000m2 MANUFACTURING FACILITIES Our Manufacturing Facilities Our manufacturing facilities are located in a closed area of 31,000 m2 constructed on a total area of 26,500 m2 in Esenyurt, istanbul. Bicakcilar offers a wide range of medical products from sterile disposable devices to medical equipment. The production of disposable medical devices is carried out in a total of 4.226 m2 clean rooms. Sterilization safety is ensured by keeping the biological load of the products under control in clean rooms. Ethylene oxide gas is used in sterilization process. Sterilization assurance is provided...

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Bicakcilar-Medical Disposable Catalog 12th Edition - 7

Bicakcilar Quality System complies with ISO 9001, EN ISO 13485 and ISO 14001 has been certified by TUV NORD and TUV THURINGEN. Bicakcilar products are CE marked. The company globalized as a brand that is relied upon and cared by the world that cares about health. Bicakcilar medical equipment and disposable products are produced according to GMP, with latest technologies in modern production facilities established on 26.500 m2 land with 30.900 m2 closed area. Biocompatible raw materials used in production are in conformity to USP and ISO 10993 Standards. In-house acceptance controls are also...

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Bicakcilar-Medical Disposable Catalog 12th Edition - 9

Turquality® TURQUALITY® is an ambitious project associated with bringing “Turkey" and “Quality" concepts together. The project is initiated by the Turkish Government, Ministry of Economy, Turkish Exporters' Assembly (TIM), and Istanbul Textile and Apparel Exporters' Association (ITKIB). The initial legal framework was laid out publicly on January 1 2th, 2004. TURQUALITY® is basically an accreditation system, which is designed not only for elevating the beneficiary companies to the level of international benchmarks, but also creating awareness on the internationally accepted values like...

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Bicakcilar-Medical Disposable Catalog 12th Edition - 10

R&D Activities “Research, Development and Creative Thinking" are the milestones of the anticipated growth in the future. We have a solid R&D infrastructure that follows the improving and changing world and industry, and develops new product designs to offer the best product in optimum quality and at the best price. R&D is the most significant element of company's mission and vision, and the primary unit that receives the largest amount of investment in Bicakcilar. Along with the new product developments in disposable devices and electro-medical equipment, and strengthening and expansion of...

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Bicakcilar-Medical Disposable Catalog 12th Edition - 11

Each stage of manufacturing is under the control of Bicakcilar Quality Control Laboratory, which employs specialized staff working in line with the GLP rules, and modern equipment. This laboratory is accredited by Turkish Accreditation Institution (TURKAK). Due to changing regulatory environment in healthcare industry both in Turkey and the world, Bicakcilar Laboratory started to comply with all articles of ISO 17025 Standard in order to offer its know-how to the use of other Medical Device Manufacturers. Chemical Test Laboratory commenced its operation as of January 2005. Bicakcilar...

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Bicakcilar-Medical Disposable Catalog 12th Edition - 13

Social Responsibility and Environment Adopting increased environmental awareness, and protection of environment as main principles, Bicakcilar Management established an Environmental Management System in order to conform manufacturing and operation to the environmental policy and targets. Bicakcilar Occupational Health and Safety- Environment Management System has been designed and documented in conformity with the terms of ISO 14001:2009 and OHSAS 18001:2007 Standards. Compliance of Environment Management System with these standards is maintained while its efficiency is constantly...

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Bicakcilar-Medical Disposable Catalog 12th Edition - 14

In line with the sustainable development principle, Bicakcilar constantly keeps environmental effects under control in order to leave a clean and healthy world to the next generations. Bicakcilar is the the first medical device manufacturing company in Turkey that has established an ethylene oxide treatment facility that operates through catalytic oxidation for the sterilization unit air emission. Thanks to its waste management activities that reduce waste production in its own source, Bicakcilar stores operational waste in its waste repositories that are specially designed for each waste...

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Bicakcilar-Medical Disposable Catalog 12th Edition - 15

ingle use medical devices have to comply with 2 EE irective if hospitals clean re package and re sterili e these devices with the intention to re use on other patients by definition the hospital becomes a medical device manufacturer Re processed single use medical devices have to be labeled in conformity with relevant standards and also instructions for use have to be provided ospitals neither are medical device manufacturers nor do they carry the responsibilities of manufacturers herefore hospital administration will be held responsible for any disease in ury and or death of a patient user...

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Bicakcilar-Medical Disposable Catalog 12th Edition - 16

DEHP-free production Unplasticised PVC is hard and brittle at room temperature. A plasticiser, softener, is typically added to increase flexilibility of the polymer. Virtually all medical devices made from PVC utilise one plasticizer: DEHP. It has been known for a long time that DEHP can leach out of PVC, resulting in exposure to body tissues and fluids. The amount of DEHP that will leach out depends on temperature, the lipid content of the liquid and the duration of contact with the plastic. It has been known that according to in vivo and in vitro research studies; DEHP or its metabolites...

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