202113 is an odious number, because the sum of its binary digits is odd. The sum of its prime factors is 1344 (or 1341 counting only the distinct ones). The product of its (nonzero) digits is 12, while the sum is 9. The square root of 202113 is about 449.5697943590. The cubic root of 202113 is about 58.6855820262. Adding to 202113 its reverse (311202), we get a palindrome (513315). The spelling of 202113 in words is "two hundred two thousand, one hundred thirteen".

If you are submitting a registration for a custom-made active implantable device, MHRA requests that you to provide us with a copy of the instructions for use and the device labelling.

For more information about this, and the steps you would need to take to rely on an expired CE certificate that has been deemed valid under the EU MDR please see the following guidance:

Please note that we now ask for more detailed information on your devices and products and request that you upload conformity assessment documents.

This is applicable to devices that are intended by the manufacturer to be sterilised before use. Manufacturers of systems and procedure packs are required to:

UK Responsible Person or Northern Ireland Authorised Representative name and address is displayed within the manufacturer record (if applicable).

Adding to 202113 its reverse (311202), we get a palindrome (513315). The spelling of 202113 in words is "two hundred two thousand, one hundred thirteen".

You need to register if your company sterilises, to place on the market under your own name, a system or procedure pack, which contains devices bearing any of the following marks:

202113 is a wasteful number, since it uses less digits than its factorization. 202113 is an odious number, because the sum of its binary digits is odd. The sum of its prime factors is 1344 (or 1341 counting only the distinct ones). The product of its (nonzero) digits is 12, while the sum is 9. The square root of 202113 is about 449.5697943590. The cubic root of 202113 is about 58.6855820262. Adding to 202113 its reverse (311202), we get a palindrome (513315). The spelling of 202113 in words is "two hundred two thousand, one hundred thirteen".

In March 2023, the EU revised the EU MDR transitional arrangements to extend the validity of EU MDD and EU AIMDD CE certificates in limited circumstances for certain medical devices. Such certificates can be relied on for placing a medical device on the Northern Ireland and Great Britain markets until the dates set out in the guidance linked below.

If you are registering a Coronavirus (COVID-19) test kit with the MHRA please take note of our guidance for industry and manufacturers.

The square root of 202113 is about 449.5697943590. The cubic root of 202113 is about 58.6855820262. Adding to 202113 its reverse (311202), we get a palindrome (513315). The spelling of 202113 in words is "two hundred two thousand, one hundred thirteen".

Manufacturers based outside Northern Ireland or the EU are required to appoint an EU or Northern Ireland based Authorised Representative if they wish to place devices on the Northern Ireland market.

It is a pernicious number, because its binary representation contains a prime number (7) of ones. It is a polite number, since it can be written in 11 ways as a sum of consecutive naturals, for example, 508 + ... + 813. It is an arithmetic number, because the mean of its divisors is an integer number (25779).

In Great Britain devices must conform to the Medical Devices Regulations 2002 (SI 2002 No 618, as amended) (UK MDR 2002) as they apply in Great Britain so that they can be placed on the market and registered with the MHRA.

This requirement does not apply to manufacturers placing Class I medical devices or general IVDs (that are not for self-testing) on the Northern Ireland market in cases where:

Custom-made devices under the EU Medical Devices Directive (EU MDD) (93/42/EEC) or EU Active Implantable Medical Devices Directive (AIMDD) (90/385/EEC) can no longer be placed on the GB market. Please note that you can register your custom-made device under UK MDR 2002 Part II or Part III (which is currently consistent with EU MDD and EU AIMDD requirements) for the GB market only, with a suitable accompanying custom-made statement.

The screenshots in the reference guides may not exactly match the latest screens in the system. Changes will be updated in the guides as soon as possible. Always follow the system on-screen messages and information.

It is a Harshad number since it is a multiple of its sum of digits (9). It is a junction number, because it is equal to n+sod(n) for n = 202095 and 202104. It is not an unprimeable number, because it can be changed into a prime (202183) by changing a digit. It is a pernicious number, because its binary representation contains a prime number (7) of ones. It is a polite number, since it can be written in 11 ways as a sum of consecutive naturals, for example, 508 + ... + 813. It is an arithmetic number, because the mean of its divisors is an integer number (25779).

Custom-made devices registered under the EU MDD or EU AIMDD and placed on the market in an EU member state other than Northern Ireland, prior to 26 May 2021, can still be registered with MHRA for the purposes of placing on the NI market only.

MHRA uses terminology to describe devices and classification per the International Medical Device Regulators Forum (IMDRF), see: Common Data Elements for Medical Device Identification.

We have prepared guidance on registration of certain medical devices which are EU MDD Class I medical devices which are a) reusable surgical instruments or b) upclassified under EU MDR.

The MHRA will only accept registration of devices from manufacturers or UK Responsible Persons that are based in the UK, or from Authorised Representatives based in Northern Ireland (for the purposes of the Northern Ireland market).

You will not be regarded as registered with the MHRA until you have provided details of the device you are registering and have received confirmation that your device is registered. You must ensure all information registered with the MHRA is accurate and up to date. We may request additional technical documentation from you to demonstrate your products conform to the relevant regulatory requirements before your registration is confirmed.

All medical devices, including IVDs, custom-made devices and systems or procedure packs must be registered with the MHRA before they can be placed on the Great Britain market.

The sum of its prime factors is 1344 (or 1341 counting only the distinct ones). The product of its (nonzero) digits is 12, while the sum is 9. The square root of 202113 is about 449.5697943590. The cubic root of 202113 is about 58.6855820262. Adding to 202113 its reverse (311202), we get a palindrome (513315). The spelling of 202113 in words is "two hundred two thousand, one hundred thirteen".

Where an EU-based Authorised Representative is appointed, the Great Britain-based manufacturer must register all device classes other than Class I devices and general IVDs (that are not for self-testing) with the MHRA.

202113 has 12 divisors (see below), whose sum is σ = 309348. Its totient is φ = 126720. The previous prime is 202109. The next prime is 202121. The reversal of 202113 is 311202.It is a happy number. It can be written as a sum of positive squares in 2 ways, for example, as 173889 + 28224 = 417^2 + 168^2 .It is not a de Polignac number, because 202113 - 22 = 202109 is a prime. It is a Harshad number since it is a multiple of its sum of digits (9). It is a junction number, because it is equal to n+sod(n) for n = 202095 and 202104. It is not an unprimeable number, because it can be changed into a prime (202183) by changing a digit. It is a pernicious number, because its binary representation contains a prime number (7) of ones. It is a polite number, since it can be written in 11 ways as a sum of consecutive naturals, for example, 508 + ... + 813. It is an arithmetic number, because the mean of its divisors is an integer number (25779).

Custom-made devices under the EU MDD or EU AIMDD can no longer be placed on the GB or NI market. Please note that you can register your custom-made device under UK MDR 2002 Part II or Part III (which is currently consistent with EU MDD or EU AIMDD requirements) for the GB market only, with a suitable accompanying custom-made statement.

In vitro diagnostic medical devices registered as undergoing performance evaluation study are not published on this database.

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Under regulation 34A of the Medical Devices Regulations 2002 no antigen or molecular detection COVID-19 (SARS-CoV-2) test may be placed on the UK market without first being validated against minimum performance standards through a Coronavirus Test Device Approvals desktop review. Persons wishing to supply, put into service or place on the UK market a coronavirus test device, need to apply to the UK’s Health Security Agency (UKHSA) for approval.

Failure to register your devices will mean that you are unable to lawfully place your device on the Great Britain market.

Great Britain manufacturers must designate an Authorised Representative based in the EU or Northern Ireland in order to place a device on the Northern Ireland market.

Please note that the accounts of any former Great Britain-based Authorised Representatives that have not updated their role to UK Responsible Person on the MHRA registration system, as well as the accounts of any represented manufacturers, have been suspended since 1 January 2022 until the UK Responsible Person has updated their role.

Non-UK manufacturers are not required to appoint a UK Responsible Person for the purpose of placing medical devices on the Northern Ireland market.

You should review your registration frequently to make sure it is up to date. It is a legal requirement to inform MHRA of any changes to your registration per regulation 7A (general medical devices), regulation 33A (in vitro diagnostic medical devices) and regulation 21A (active implantable medical devices) of the Medical Devices Regulations (2002) (SI 2002 No 618) (as amended) concerning registration of persons placing medical devices on the Great Britain market, as and when they occur. Please do not wait for reminder emails.

You are asked to provide the following information when registering your devices with us. Please note these lists are non-exhaustive and we may request further technical documentation from you as part of our scrutiny and data validation process.

The video tutorial screens may not exactly match the latest screens in the system. Changes will be updated in the videos as soon as possible. Always follow the system on-screen messages and information.

We have introduced legislation to supplement provisions that were introduced in Northern Ireland on 26 May 2021 when the EU Medical Devices Regulation (2017/745) (EU MDR) took effect. This legislation has introduced a requirement to register all custom-made devices with the MHRA within 28 days of being made available on the Northern Ireland market.

You can register up to 100 devices (GMDN®) with a cumulative maximum of 20,000 products (medical device brand/trade/proprietary name, model/version, catalogue/reference, UDI-DI etc.) within each application.

Where a Northern Ireland-based Authorised Representative is appointed, the Authorised Representative must register all devices with the MHRA.

If your registration is not displaying on PARD or your devices are displaying as ‘Devices pending update by manufacturer’, please access your account and take any necessary action to bring your registration up to date. Please see Review registration and Making Changes to your registration.

Updated 'Account Management Reference Guide' & 'Device Registration Reference Guide' to reflect changes to the registration system.

Updated guidance on registration of certain medical devices which are reusable Class I devices, upclassified Class I devices, and/or reliant on expired/expiring CE certificates.

There is currently a requirement to register with the MHRA, certain medical devices (including IVDs, custom-made devices and systems and procedure packs) that are placed on the Northern Ireland market.

The product of its (nonzero) digits is 12, while the sum is 9. The square root of 202113 is about 449.5697943590. The cubic root of 202113 is about 58.6855820262. Adding to 202113 its reverse (311202), we get a palindrome (513315). The spelling of 202113 in words is "two hundred two thousand, one hundred thirteen".

In some circumstances, it is a requirement of the UK MDR 2002 that you inform the MHRA when you first place your device on the Northern Ireland market. The precise requirements depend on the location of the manufacturer, the location of the Authorised Representative and the device class. Please see below for further information.

It is not a de Polignac number, because 202113 - 22 = 202109 is a prime. It is a Harshad number since it is a multiple of its sum of digits (9). It is a junction number, because it is equal to n+sod(n) for n = 202095 and 202104. It is not an unprimeable number, because it can be changed into a prime (202183) by changing a digit. It is a pernicious number, because its binary representation contains a prime number (7) of ones. It is a polite number, since it can be written in 11 ways as a sum of consecutive naturals, for example, 508 + ... + 813. It is an arithmetic number, because the mean of its divisors is an integer number (25779).

All medical devices, including IVDs, custom-made devices and systems or procedure packs, must be registered with the MHRA before they can be placed on the market in Great Britain (England, Wales and Scotland).

Registration of your devices with the MHRA (the UK Competent Authority) does not represent any form of accreditation, certification, approval or endorsement by the MHRA.

Once registered, your company name, address and registered medical device types are added to the Public Access Registration Database (PARD) for medical device registration.

Systems and procedure packs are covered by the registration requirements set out above. You need to register if your company places on the market a system or procedure pack under your own name, and within the intended purposes and limits specified by the manufacturer, which contains devices bearing any of the following marks:

As part of our data validation and scrutiny of applications to register medical devices and products with the MHRA, we may request further technical documentation from you that demonstrates your products conform to the requirements of the Medical Device Regulations.

If you are already registered with us and have a question about your registration details email device.registrations@mhra.gov.uk quoting your reference number.

If any changes need to be made to organisation details or new devices need to be added to your registration/s these are separate transactions that incur the statutory fee per application. Please note, if organisation name and/or address has changed you must update these before renewing your registration, you cannot do this within the Renew Registration application. Follow the instructions for Editing Organisation details in the , the fee is payable.

The UK Responsible Person will then assume the responsibilities of the manufacturer in terms of registering the device with the MHRA.

202113 is a deficient number, since it is larger than the sum of its proper divisors (107235). 202113 is a wasteful number, since it uses less digits than its factorization. 202113 is an odious number, because the sum of its binary digits is odd. The sum of its prime factors is 1344 (or 1341 counting only the distinct ones). The product of its (nonzero) digits is 12, while the sum is 9. The square root of 202113 is about 449.5697943590. The cubic root of 202113 is about 58.6855820262. Adding to 202113 its reverse (311202), we get a palindrome (513315). The spelling of 202113 in words is "two hundred two thousand, one hundred thirteen".

However, please note that GMDN® is a worldwide system and not all of its codes and terms are considered to be medical devices in the UK. If you would like further guidance on whether certain products are medical devices in the UK, please see Borderline products: how to tell if your product is a medical device.

If you do not know which GMDN® Code applies to your device, you will be able to select the relevant Term from our system. You do not need to be a member of the GMDN® Agency to find and select the appropriate GMDN® Terms in our online registration system (DORS).

Changes to DORS instructions for Scenarios 1 to 4 in the Guidance on registration of medical devices with an expired or expiring CE Certificate.

Therefore, you are not permitted to make any claims to this effect, including the use of any MHRA logos in any marketing materials, on device packaging, in the instructions for use, on laboratory tickets/dockets, or in any other documentation.

If you do not review your registration and submit the Renew registration application your account will be suspended. Suspended accounts are removed from the Public Access Registration Database (PARD) and you will not be able to add new devices or order Certificates of Free Sale until you have reviewed your registration and submitted the renewal application.

If you are registering devices as a UK Responsible Person or a Northern Ireland-based Authorised Representative, you also need to provide details of the manufacturer(s) you are representing. The above device registration process will then apply.

This guidance has been updated now that the Government has made regulations that enable CE marked medical devices to continue to be accepted in Great Britain for defined periods beyond 30 June 2023.

Reference guides and the videos 'update devices and update products individually' and 'review and renew registration' have been updated.

It is a junction number, because it is equal to n+sod(n) for n = 202095 and 202104. It is not an unprimeable number, because it can be changed into a prime (202183) by changing a digit. It is a pernicious number, because its binary representation contains a prime number (7) of ones. It is a polite number, since it can be written in 11 ways as a sum of consecutive naturals, for example, 508 + ... + 813. It is an arithmetic number, because the mean of its divisors is an integer number (25779).

This contains information to be aware of if you are registering the following types of medical devices with MHRA as self-declared as meeting requirements in EU MDD:

It is not an unprimeable number, because it can be changed into a prime (202183) by changing a digit. It is a pernicious number, because its binary representation contains a prime number (7) of ones. It is a polite number, since it can be written in 11 ways as a sum of consecutive naturals, for example, 508 + ... + 813. It is an arithmetic number, because the mean of its divisors is an integer number (25779).

Any fees referred to in the video tutorials are for demonstration purposes only. Please refer to the Fees section for current fees.

If the manufacturer is based outside of the UK, they must appoint a single UK Responsible Person to take responsibility for all of their medical devices.

We have implemented a renew registration process as a reminder to review your registration and confirm that it is up to date. The first renewal date is 1 year after account request was completed by MHRA, and then at least every 2 years. You will receive automated email reminders 3, 2 and 1 month before your renewal date – you can review and submit the Renew registration application from 3 months before the renewal date. There is currently no fee for this application.

Updates to the Review Registration, Making Changes to your registration and Public Register of Manufacturers sections. Updated Account Management and Device Registration Reference Guides.

Therefore, you are not permitted to make any claims to this effect, including the use of any MHRA logos in any marketing materials, on device packaging, in the instructions for use, on laboratory tickets/dockets, or in any other documentation.

The Northern Ireland-based Authorised Representative must provide the MHRA with details of the person placing the product on the Northern Ireland market if the person placing the product on the market is not:

Registration applications for covid test devices will not be accepted by the MHRA until the devices have received Coronavirus Test Device Approval (CTDA) or are placed onto the Temporary Protocol list. If you believe your Covid test device is exempt from the approval requirements and wish to register it with MHRA, it is probable you will be contacted to specify the exemption applicable under the Medical Devices Regulations 2002 (as amended by The Medical Devices (Coronavirus Test Device Approvals) (Amendment) Regulations 2021 before your MHRA registration application is accepted.

It can be written as a sum of positive squares in 2 ways, for example, as 173889 + 28224 = 417^2 + 168^2 .It is not a de Polignac number, because 202113 - 22 = 202109 is a prime. It is a Harshad number since it is a multiple of its sum of digits (9). It is a junction number, because it is equal to n+sod(n) for n = 202095 and 202104. It is not an unprimeable number, because it can be changed into a prime (202183) by changing a digit. It is a pernicious number, because its binary representation contains a prime number (7) of ones. It is a polite number, since it can be written in 11 ways as a sum of consecutive naturals, for example, 508 + ... + 813. It is an arithmetic number, because the mean of its divisors is an integer number (25779).

In such cases, the UK Responsible Person or the manufacturer must provide the MHRA with the importer details, including their place of business in Great Britain.

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Please ensure that payments for device registration applications are only made through the Device Online Registration System (DORS) .

As set out in that guidance, you will need to complete and upload the following template letter: EU MDR Article 120 Extension Confirmation Template.

2202113 is an apocalyptic number. It is an amenable number. 202113 is a deficient number, since it is larger than the sum of its proper divisors (107235). 202113 is a wasteful number, since it uses less digits than its factorization. 202113 is an odious number, because the sum of its binary digits is odd. The sum of its prime factors is 1344 (or 1341 counting only the distinct ones). The product of its (nonzero) digits is 12, while the sum is 9. The square root of 202113 is about 449.5697943590. The cubic root of 202113 is about 58.6855820262. Adding to 202113 its reverse (311202), we get a palindrome (513315). The spelling of 202113 in words is "two hundred two thousand, one hundred thirteen".

This guidance was updated to include information on the registration of certain CE marked medical devices in scope of transitional arrangements under the EU Medical Devices Regulation. It was also updated to reflect an intended extension to acceptance of CE marked medical devices on the Great Britain market beyond 30 June 2023.

It is a happy number. It can be written as a sum of positive squares in 2 ways, for example, as 173889 + 28224 = 417^2 + 168^2 .It is not a de Polignac number, because 202113 - 22 = 202109 is a prime. It is a Harshad number since it is a multiple of its sum of digits (9). It is a junction number, because it is equal to n+sod(n) for n = 202095 and 202104. It is not an unprimeable number, because it can be changed into a prime (202183) by changing a digit. It is a pernicious number, because its binary representation contains a prime number (7) of ones. It is a polite number, since it can be written in 11 ways as a sum of consecutive naturals, for example, 508 + ... + 813. It is an arithmetic number, because the mean of its divisors is an integer number (25779).

It is a polite number, since it can be written in 11 ways as a sum of consecutive naturals, for example, 508 + ... + 813. It is an arithmetic number, because the mean of its divisors is an integer number (25779).

If you are already registered with the MHRA, we encourage you to make the necessary changes to your registered information as and when they occur. Please do not wait for reminder emails.

You also need to provide a copy of any conformity assessment certificates or self-certification conformity declarations, as applicable.

Please review organisation details and all registered devices and products and take the necessary action to ensure the data is correct and up to date. Please follow the Manage Registered Devices instructions in the and watch the video tutorial for steps on how to review your devices and take any necessary action. This includes uploading new Conformity documents, adding or removing products, adding devices, or removing devices (that you no longer manufacture, or migrated devices with Pseudo Global Medical Device Nomenclature (GMDN®), where applicable).

Custom-made devices registered under the EU MDD or EU AIMDD and placed on the market in an EU member state other than Northern Ireland, prior to 26 May 2021, can still be registered with MHRA for the purposes of placing on the NI market only.

Please contact the MHRA by emailing Device.Registrations@mhra.gov.uk for advice on how to register your custom-made devices if:

It is an amenable number. 202113 is a deficient number, since it is larger than the sum of its proper divisors (107235). 202113 is a wasteful number, since it uses less digits than its factorization. 202113 is an odious number, because the sum of its binary digits is odd. The sum of its prime factors is 1344 (or 1341 counting only the distinct ones). The product of its (nonzero) digits is 12, while the sum is 9. The square root of 202113 is about 449.5697943590. The cubic root of 202113 is about 58.6855820262. Adding to 202113 its reverse (311202), we get a palindrome (513315). The spelling of 202113 in words is "two hundred two thousand, one hundred thirteen".

In cases where the Great Britain importer is not the UK Responsible Person, the importer must inform the relevant manufacturer or UK Responsible Person of their intention to import a device.

The previous prime is 202109. The next prime is 202121. The reversal of 202113 is 311202.It is a happy number. It can be written as a sum of positive squares in 2 ways, for example, as 173889 + 28224 = 417^2 + 168^2 .It is not a de Polignac number, because 202113 - 22 = 202109 is a prime. It is a Harshad number since it is a multiple of its sum of digits (9). It is a junction number, because it is equal to n+sod(n) for n = 202095 and 202104. It is not an unprimeable number, because it can be changed into a prime (202183) by changing a digit. It is a pernicious number, because its binary representation contains a prime number (7) of ones. It is a polite number, since it can be written in 11 ways as a sum of consecutive naturals, for example, 508 + ... + 813. It is an arithmetic number, because the mean of its divisors is an integer number (25779).

Custom-made devices registered under the EU MDD or EU AIMDD and placed on the market in an EU member state other than Northern Ireland, prior to 26 May 2021, can still be registered with MHRA for the purposes of placing on the NI market only.

It is a requirement of the UK MDR 2002 that you inform the MHRA before you place your device on the market in Great Britain.

Since 1 January 2021, there have been requirements for non-UK manufacturers to have a UK Responsible Person for the purposes of registering devices placed on the Great Britain market. A Northern Ireland-based Authorised Representative can no longer register devices on a manufacturer’s behalf for the Great Britain market.

Registration of your devices with the MHRA (the UK Competent Authority) does not represent any form of accreditation, certification, approval or endorsement by the MHRA.

If you registered with the MHRA before 1 July 2018 and have a registration number that begins with ‘CA, or IVD’ or your registration does not appear on the Public Access Registration Database (PARD) you will need to re-register your organisation details and devices on the DORS system.

How to register your medical devices with the Medicines and Healthcare products Regulatory Agency (MHRA) for the markets in Great Britain and Northern Ireland

If no changes need to be made, you will not currently be charged for this review. Please follow the Renew Registration instructions in the and watch the Renew Registration video tutorial.

If you have any queries or complaints about the registration process, please email device.registrations@mhra.gov.uk, quoting your reference number.

This guidance has been updated to reflect changes to medical device registration requirements that will take effect on 1 January 2022.

Please note that new requirements have been introduced regarding the registration of custom-made devices in Northern Ireland. Please see below for further information.

Please update any data fields that were not previously populated by following the Update registered devices and products instructions in the and watch the video tutorial. In particular we urge you to provide the UDI-DIs for your devices (where applicable) as these will be crucial for monitoring and ensuring patient safety.