Health Products Medical Devices Regulations 2022

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Health Products (Medical Devices) (Amendment No. 2) …

https://sso.agc.gov.sg/SL-Supp/S950-2022/Published/20221209?DocDate=20221209

3D.—. (1) Subject to paragraphs (3) and (4), a person may manufacture a specified dental medical device without holding a manufacturer’s licence under section 12 (1) of the Act if —. ( a) the person does not manufacture any medical device that is not a …

2022 Device Approvals | FDA - U.S. Food and Drug …

https://www.fda.gov/medical-devices/recently-approved-devices/2022-device-approvals

2022 Device Approvals. The products listed in this section include some of the newest medical technology from the year 2022. The products in each list contain information …

Medical devices - World Health Organization

https://www.who.int/health-topics/medical-devices

Policies, strategies, and action plans for health technologies, specifically for medical devices, are required in any national health plan. Within the context of a robust …

Health Products (Medical Devices) Regulations 2010

https://sso.agc.gov.sg/SL/HPA2007-S436-2010

No. S 436. Health Products Act. (Chapter 122D) Health Products (Medical Devices) Regulations 2010. In exercise of the powers conferred by sections 45, 71 and 72 of the …

Medical Devices - New regulations - Public Health

https://health.ec.europa.eu/medical-devices-new-regulations_en

26 May 2022, the Regulation (EU) 2017/746 on In Vitro Diagnostic Medical Devices is applicable within the EU. News announcement.

New Regulations - Public Health

https://health.ec.europa.eu/medical-devices-sector/new-regulations_en

Regulation (EU) 2022/112 of the European Parliament and the Council of 25 January 2022 introduced a staggered extension of the transition periods provided for in Regulation (EU) …

Medical devices - Canada.ca

https://www.canada.ca/en/health-canada/services/drugs-health-products/medical-devices.html

Summary reporting provisions of the Medical Devices Regulations: Notice to industry [2022-11-21] Medical devices contained in electronic health record (EHR) …

Factsheet: medical devices overview

https://www.gov.uk/government/publications/medicines-and-medical-devices-bill-overarching-documents/factsheet-medical-devices-overview

A medical device is any apparatus, appliance, software, material or other article, whether used alone or in combination, intended by the manufacturer to be used by …

Medical Devices Regulations ( SOR /98-282) - laws …

https://laws-lois.justice.gc.ca/eng/regulations/SOR-98-282/

43.1 - Obligation to Submit Certificate. 43.11 - Disclosure of Information in Respect of Clinical Studies or Investigational Testing. 43.2 - Medical Devices to Be Sold for the Purposes of …

MEDICAL DEVICE GUIDANCE - Health Sciences …

https://www.hsa.gov.sg/docs/default-source/hprg-mdb/gn-12-2-r2-guidance-on-grouping-specific-(2022-jan)-pub.pdf

JANUARY 2022 MEDICAL DEVICE GUIDANCE . GN-12-2: Guidance on Grouping of Medical Devices ... the registration requirement has been provided for in the …

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