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Books on Demand CE-Marking

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Last 637 days • 637 data points (No recent data available)

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£56.90 £36.53 £40.97 £45.42 £49.86 £54.31 £58.75 09 June 2024 15 November 2024 23 April 2025 29 September 2025 07 March 2026

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30 days 117 days 36 days · current 62 days 68 days 324 days 0 81 162 243 324 £38 £39 £40 £54 £55 £57 Days at Price

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Most common price: £57 (324 days, 50.9%)

Price range: £38 - £57

Price levels: 6 different prices over 637 days

Description

The development of medical technology in the last years of the 20th century has been very dynamic. Synthetic single-use products, artificial joint replacements, pacemaker technologies or minimal-invasive procedures result in a high standard of medical care. But despite of the huge progress in this field, we are presumably only at the beginning of a medical technology revolution. The 1st version of the German Medizinproduktegesetz (MPG, Medical Devices Act) came into effect on January 1, 1995. It represents the national implementation of the European directives 90/385/EEC for active implantable medical device, 93/42/EEC for medical devices and 98/79/EEC for in vitro diagnostic devices. With the implementation of this act in the EU internal market, the free movement of medical devices was established. Medical devices that are marketable in one member state of the EU are also marketable in the other EU countries. Manufacturers of medical devices can therefore place their products on the whole EU market. The CE-mark on the products is the proof of complying with the essential requirements. The Medical Devices Act guarantees the efficacy and safety of the medical device because the product has to undergo comprehensive control procedures during the design and manufacturing process. The CE-mark is a cachet for quality and efficacy. After the market access, the authorities take care of the safety for users and consumers via definition of essential requirements. This book presents the major aspects of the Medical Devices Act and the European directives. Moreover, the responsibilities and duties of a medical device manufacturer are explained as well as the product classifications and what the manufacturer has to keep in mind when designing and producing medical devices that comply with the legal requirements. A lot of physicians implant medical devices without being aware of the highly complex registration landscape. Especially in clinical research, the regulations regar

Product Specifications

Format
paperback
Domain
Amazon UK
Release Date
26 January 2015
Listed Since
27 January 2015

Barcode

No barcode data available

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