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Used in operating theaters throughout the local market and overseas,
Sion Biotext procedure packs are designed and manufactured according to a full quality assurance system accredited to ISO 9001: 2000, and ISO 13485: 2003. In addition, the medical device pack components are CE marked and sterilised in accordance with the manufacturers instructions as stipulated in the Medical Device Directive (93/42/EEC).
Our extensive experience ensures a full understanding of the specific needs of the hospital staff.
Sion Biotext Medical is proud of its reputation in the healthcare market and of its long-standing commitment to providing an efficient and responsive service to all customers.
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