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BackgroundAn optimal surgical environment can only be achieved by treating the operation theatre as a coherent unit in order to reduce the risk of post-operative infections and minimise the risk of infections transmitted by blood. Since the preliminary testing in Denmark and Sweden, TEXguardŽ clothing has been based on the concept of satisfying comfort, safety, environment and cost optimisation requirements - but without "completely overdoing it". Several years of tests have created the TEXguardŽ concept, the best possible clothing for the operation theatre. The materialThe TEXguardŽ concept now uses the Swedish Cambric fabric with its unique and
durable liquid-repellent surface, ideal for staff, patients and laundry washing. |
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| The Cambric fabric's surface tension is suitable for all the liquids normally encountered during surgery. Products made of Cambric will, therefore, serve as liquid-repellent barriers during normal or dry operations. |
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Cambric is a closely woven polyester/cotton textile. Unlike alternative fabrics and disposable materials, it provides a high level of comfort as well as an adequate barrier against liquids and bacteria transmitted by air. The test results below bear witness to its qualities:
To satisfy everybody's needs, the TEXguardŽ concept contains a number of other
well-known materials, such as microfibres, 100% polyester and two-layer and three-layer
laminates. |
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ProductsThe TEXguardŽ concept includes a number of models that fulfil requirements for:
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The TEXguardŽ surgical gown has an overlapping back and raglan sleeves. The design of the gown means that it is a good fit for just about any build. |
| The TEXguardŽ scrub suit is designed for use during operations, acting as a fluid and bacteria barrier and extremely working comfortable to work in. | ![]() |
All the products in the range are produced according to individual customer requirements and specifications. ApprovalsThe TEXguardŽ products are produced under controlled, consistent conditions as described in Kay Borch A/S' own quality assurance system. Since 25 August 1998, TEXguardŽ products have complied with the conditions laid down by the Council directive of 14 June 1993 on medical regulations (93/42/EEC). The CE marking is accompanied by a formal reporting system with:
TEXguardŽ surgical gowns also bear a 510(K) pre-market notification approval by the Food and Drug Administration (FDA) allowing sale and distribution of the products in USA. |
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