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RG2 registration form. April 2014. Page 1 of 12. Competent Authority (UK). Medical Devices Regulations 2002 No. 618, Regulations 19 and 30. Form RG2 Guidance on Completing an RG2 Form for Medicines and Healthcare Products. Regulatory Agency (MHRA) Registration. This guidance has been developed for COMPETENT AUTHORITY (UK) MEDICAL DEVICES REGULATIONS 2002: REGULATION 19 FORM RG2 REGISTRATION OF PERSONS RESPONSIBLE FOR Guidance on Completing an RG2 Form for Medicines and Healthcare Products Regulatory Agency (MHRA) Registration This guidance has been developed for their details with the UK Competent Authority MHRA, however they may wish to and can do so by completing the RG2 form. In addition to the completed form, When registering with the MHRA a Class 1 Medical Device using the RG2 form, do you need to supply any product information or device MEDICAL DEVICES REGULATIONS 2002: REGULATIONS 19 and 30. FORM RG2. REGISTRATION OF PERSONS RESPONSIBLE FOR PLACING DEVICES 618, Regulations 19 and 30 Form RG2 registration of medical devices For office use only Date of receipt Evidence in support of application checklist Y/N
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