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Windows 7 and later. Click Start Settings Control Panel. Double-click Uninstall a program. Find and select Google Earth Pro. Click Uninstall. Uninstall Earth Pro on a Mac. Go to your Applications folder and search for "Google Earth Pro". Right-click the Google Earth Pro icon and select Move to Trash.

Руководство по эксплуатации инкубатора тромбоцитов

0086 СЕРТИФИКАТ ISO 13485:2003 Руководство по эксплуатации инкубатора тромбоцитов i.Series® и Horizon Series™ 360093-1/P Модельный ряд i.Series Horizon Series Настольный PC100i, PC900i, PC1200i (Версия A) PC100h, PC900h, PC1200h (Версия A)

CE-Marking: The Full Guide For Selling Products In The EU

The CE marking has a height of at least 5 millimetres. The CE marking is placed onto the product or to its data plate. When the size of the product does not allow this, the marking can be placed onto the packaging or in accompanying documents, such as the user manual. The CE marking is easily visible, readable and permanent.

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CE Circular economy CEAP Circular Economy Action Plan (EU) CEFSP Circular Economy Finance Support Platform (EU) CEM European Circular Economy Mission CEN European Committee for Standardization CENELC European Committee for Electrotechnical Standardization CEO Chief executive officer CEREWG Resource Efficiency Working Group (EU) CRM Critical raw ...

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CE marking - GOV.UK

Overview. The letters 'CE' appear on many products that are traded on the single market in the European Economic Area (EEA). The CE marking is …

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List of Notified bodies accredited for Medical Device CE ...

A notified body is an organization that has been accredited by an EU Member State to conduct a conformity assessment under the relevant EU Directives and issue CE certificate. After certification manufacturers can affix CE Mark on their Medical device and are free to market their devices in all EU Member states. Manufacturers can choose any notified body for conformity assessment (audit ...

ISO 13485 — Википедия

Требования для целей регулирования». ISO 13485 — международный отраслевой стандарт, разработанный Международной организацией по стандартизации. Стандарт содержит требования к …

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What is CE Marking? - CE Mark Certification vs. Self ...

The Conformitè Europëenne (CE) Mark is defined as the European Union's (EU) mandatory conformity marking for regulating the goods sold within the European Economic Area (EEA) since 1985. The CE marking represents a manufacturer's declaration that products comply with the EU's New Approach Directives. These directives not only apply to ...

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СЕ маркировка правила условия нанесения, экспорт, Mark, сертификация продукции в Европейском Союзе, Kennzeichnung, декларация, оценка соответствия, EC Declaration of Conformity, знак, обозначение

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BSI Migration of Certificates from UK Notified Body (0086 ...

The named manufacturer has completed migration of the enclosed CE certificate(s), originally issued by BSI UK (0086) Notified Body to BSI Group The Netherlands B.V. which is a European Notified Body designated in The Netherlands for the following three directives: MDD (93/42/EEC), AIMDD (90/385/EEC) and IVDD (98/79/EC).

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Guidelines for Classification of Medical Devices - CE ...

Other CE Publications Related to Medical Devices: 93/465/eec: Conformity Assessment Procedures & CE Marking Rules; 2001 Guidelines for Classification of Medical Devices; Guidelines relating to the demarcation between Directives 90/385/eec, 93/42/eec and 65/65/eec.

ISO - ISO 14001:2015 - Environmental management systems ...

ISO 14001:2015 specifies the requirements for an environmental management system that an organization can use to enhance its environmental performance. ISO 14001:2015 is intended for use by an organization seeking to manage its environmental responsibilities in a systematic manner that contributes to the environmental pillar of sustainability.

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Medical devices | European Medicines Agency

Medical devices are products or equipment intended generally for a medical use and are regulated at Member State level. The Regulations on Medical Devices (Regulation (EU) 2017/745) and on In-Vitro Diagnostic Devices (Regulation (EU) 2017/746) changed the European legal framework for medical devices, introducing new responsibilities for the European Medicines Agency (EMA) and national ...