Freedom of Information request on the statistics on how many medical devices got registered with UK MHRA after the 1st grace period of May 1st 2021 and what was the class of the device (FOI 21-782)
Published 27 April 2022
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5th August 2021 FOI 21/782
Dear
We refer to your email dated 7 July 2021.
You requested the following;
i. The statistics on how many medical devices got registered with UK MHRA after the 1st grace period of May 1st, 2021 and what was the class of the device. ii. Statistics on how many devices got registered in the month of April and from May till date.
The information you have requested is already in the public domain, and can be found at Register medical devices to place on the market - GOV.UK (www.gov.uk). You will have to go to the section entitled Public register of manufacturers. The Freedom of Information (FOI) Act’s section 21 exemption states that there is no right of access to information via FOI if it is reasonably available to the applicant by another route.
If you disagree with how we have interpreted the Freedom of Information Act 2000 with regards to your request, you can ask for the decision to be reviewed. The review will be carried out by a senior member of the Agency who was not involved with the original decision.
If you have a query about the information provided, please reply to this email.
If you disagree with how we have interpreted the Freedom of Information Act 2000 with regards to your request, you can ask for the decision to be reviewed. The review will be carried out by a senior member of the Agency who was not involved with the original decision. Internal review requests should be submitted within two months of the date you receive this response and addressed to: [email protected]
If you were to remain dissatisfied with the outcome of the internal review, you would have the right to apply directly to the Information Commissioner for a decision. Please bear in mind that the Information Commissioner will not normally review our handling of your request unless you have first contacted us to conduct an internal review. The Information Commissioner can be contacted online: https://ico.org.uk/make-a-complaint/official-information-concerns-report/official-information-concern/
Please remember to quote the reference number above in any future communications.
Yours sincerely
MHRA Customer Service Centre
Medicines and Healthcare products Regulatory Agency 10 South Colonnade, Canary Wharf, London E14 4PU