1-10 of 10 results for legtitle:"Medical Devices Regulations 2002"
Librarians' tools
- Search time
- 0.252 seconds
- Solr query time
- 0.001 seconds
- Search query
- legtitle:"Medical Devices Regulations 2002"
- We searched for
- legislationTitle_t:"Medical Devices Regulations 2002"
Type
House
Session
Year
Department
Member
Primary member
Answering member
Legislative stage
Legislation
Subject
More
Publisher
Clause 59, discussed with amendments, schedule 8, clauses 60 and 61 stand part, and new clause 42. Clause 59 agreed to on division (10 votes to 6). Amendment to schedule 8 negatived on division (4 votes to 10). Schedule 8 agreed to. Clauses 60 and 61 agreed to on division (10 votes to 4 respectively). Clauses 62 and 63 agreed to. Clause 64, discussed with schedule 9, new clauses 74 and 78. Clause 64 agreed to on division (10 votes to 6). Schedule 9 agreed to. Clause 65, discussed with schedule 10, agreed to on division (9 votes to 6). Schedule 10 agreed to. Clauses 66 and 67 agreed to. Schedule 11 agreed to, as amended. Government new clauses 20 to 23 agreed to. Government new clause 91, discussed with Government new clauses 92 to 95, Government amendments, and new clauses 67 and 68. Government new clauses 91 to 95 agreed to. New clause 1, discussed with new clause 13, debated and withdrawn. New clause 3, discussed with new clauses 4, 5, 9, 10 and 43. New clause 3 debated and withdrawn. New clause 4 negatived on division (2 votes to 8). New clause 5 negatived on division (2 votes to 8). Committee adjourned till 9 July. Written evidence reported to the House.
Clause 59, discussed with amendments, schedule 8, clauses 60 and 61 stand part, and new clause 42. Clause 59 agreed to on division (10 votes to 6). Amendment to schedule 8 negatived on division (4 votes to 10). Schedule 8 agreed to. Clauses 60 and 61 agreed to on division...
To ask the Secretary of State for Health and Social Care, how many (a) invitro diagnostic and (b) other medical devices that (i) are UK approved body certified and (b) self-declared under the Medical Devices Regulations 2002 are registered with the Medicines and Healthcare products Regulatory Agency.
To ask the Secretary of State for Health and Social Care, how many (a) invitro diagnostic and (b) other medical devices that (i) are UK approved body certified and (b) self-declared under the Medical Devices Regulations 2002 are registered with the Medicines and Healthcare products Regulatory Agency.
The information requested has been verified by the Medicines and Healthcare products Regulatory Agency (MHRA) but has not been previously published. The following table shows the number of medical devices registered with the MHRA including United Kingdom approved body certified and self-declared under Medical Devices Regulations (MDR) 2002.
| In Vitro-Diagnostic Medical Devices | General Medical Devices | Active Implantable Medical Devices | Total |
UK approved body certified | 1 | 187 | 1 | 189 |
Self-declared MDR 2002 | 1 | 169 | 0 | 170 |
Total | 2 | 356 | 1 | 359 |
The in-vitro diagnostic medical devices referenced were declared under part IV of the UK Medical Devices Regulations (MDRs) 2002, the general medical devices referenced were declared under part II of the UK MDRs 2002 and the active implantable medical devices were declared under part III of the UK MDRs 2002.
A debate has been scheduled for 4.30pm on Tuesday 28 March on medical technology regulations and the NHS. The debate will be opened by Dame Caroline Dinenage MP.
A debate has been scheduled for 4.30pm on Tuesday 28 March on medical technology regulations and the NHS. The debate will be opened by Dame Caroline Dinenage MP.
To ask the Secretary of State for Health and Social Care, with reference to the Retained EU Law Bill, whether he plans to (a) revoke, (b) retain or (c) replace the Medical Devices Regulations 2002.
To ask the Secretary of State for Health and Social Care, with reference to the Retained EU Law Bill, whether he plans to (a) revoke, (b) retain or (c) replace the Medical Devices Regulations 2002.
Through the Retained EU Law (Revocation and Reform) Bill, the Government is currently reviewing which retained European Union (EU) law should be repealed, reformed or preserved. The Government continues to work with a range of stakeholders to ensure that any such reforms maintain current standards in patient safety and public health. The Medicines and Healthcare products Regulatory Agency (MHRA) is participating in the review of all retained EU law within its responsibilities.
In parallel, we are progressing reforms to the Medical Devices Regulations 2002 under the Medicines and Medical Devices Act 2021. These are outlined in the government response to the consultation on the future regulation of medical devices in the United Kingdom published in June last year.
Protocol in accordance with regulation 39A(2) and (3) of the Medical Devices Regulations 2002. Includes Annex listing coronavirus test devices and their manufacturers. 9p.
Protocol in accordance with regulation 39A(2) and (3) of the Medical Devices Regulations 2002. Includes Annex listing coronavirus test devices and their manufacturers. 9p.
Clauses 17 to 23 agreed to. Government amendment made to clause 24. Clause 24 agreed to as amended. Schedule 1 agreed to. Clauses 25 to 45 agreed to. Government amendment made to schedule 2. Schedule 2 agreed to as amended. New Clause 6 (Registration of Medical Devices) debated and withdrawn. Bill, as amended, to be reported (Bill 136). Written evidence reported to the House.
Clauses 17 to 23 agreed to. Government amendment made to clause 24. Clause 24 agreed to as amended. Schedule 1 agreed to. Clauses 25 to 45 agreed to. Government amendment made to schedule 2. Schedule 2 agreed to as amended. New Clause 6 (Registration of Medical Devices) debated and withdrawn....
SI 2009/383. Together with an explanatory memorandum and impact assessment from the Department of Health. Coming into force 1 April 2009.
SI 2009/383. Together with an explanatory memorandum and impact assessment from the Department of Health. Coming into force 1 April 2009.
Decontamination of re-usable medical devices in the primary, secondary and tertiary care sectors (NHS and independent providers): clarification and policy summary. 8 p.
Decontamination of re-usable medical devices in the primary, secondary and tertiary care sectors (NHS and independent providers): clarification and policy summary. 8 p.
SI 2002/618 (Negative instrument). Coming into force 13 June 2002
SI 2002/618 (Negative instrument). Coming into force 13 June 2002