United Kingdom · Question · Written question
HL HL9779
Certification Quality Marks
Introduced
4 September 2023
Last action
12 September 2023 · Answer
Status
Answered
Sponsors
—
Subjects
Discovery layer
Source updated
12 September 2023
Summary
To ask His Majesty's Government why the use of both the UK Conformity Assessment mark and the EU’s CE mark will be allowed indefinitely for UK companies in the electronic, industrial, consumer and other sectors, but not for medical products produced in th
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Timeline
4 September 2023
Written question
To ask His Majesty's Government why the use of both the UK Conformity Assessment mark and the EU’s CE mark will be allowed indefinitely for UK companies in the electronic, industrial, consumer and other sectors, but not for medical products produced in th
Source: Lords
12 September 2023
Answer
Medical devices are regulated by the Medicines and Healthcare products Regulatory Agency (MHRA) and are considered high-risk goods. The Government has put in place legislation to extend the acceptance of CE marked medical devices on the Great Britain mark...
Source: Written answer
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- · Department of Health and Social Care · Answering body
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Sources
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- Official source: https://questions-statements.parliament.uk/written-questions/detail/2023-09-04/HL9779
- Open data entity: https://questions-statements-api.parliament.uk/api/writtenquestions/questions/1657615
- uk · wq-1657615 · source updated 12 September 2023