Warning Status
|
|
|---|---|
Warning Date
|
|
Manufacture Company
|
|
The Saudi Food and Drug Authority (SFDA) issued a warning regarding the safety of devices Implanted medical devices which are affected by masks containing magnets (face and nasal masks) used with Bilevel Positive Airway Pressure (BiPAP) and Continuous Positive Airway Pressure (CPAP) medical devices, produced by the Philips Respironics factory.
To report sector-related issues
Call Centre 19999
International Organization for Standardization (ISO) Technical Committee for Specifications of anaesthetic and respiratory equipment approved several proposals submitted by the Saudi Food and Drug Authority (SFDA), during the committee’s meetings held from July 11 to 15 in St. Johns, Canada.
Saudi Food and Drug Authority (SFDA) monitored 274 violations in facilities under its supervision, during 4,891 inspection tours in all regions of the Kingdom of Saudi Arabia in August this year.
The Saudi Food and Drug Authority (SFDA) participated in the annual meeting of the International Medical Device Regulators Forum (IMDRF) which was held virtually for three days and hosted by the Therapeutic Goods Administration (TGA).
SFDA was represented by the Vice President for Medical Devices Sector at SFDA and Chairman of Global Harmonization Working Party (GHWP), Eng. Ali Al-Dalaan.
Saudi Food and Drug Authority (SFDA) monitored 291 violations in facilities under its supervision, during 4,677 inspection tours in all regions of the Kingdom of Saudi Arabia in June this year.
SFDA stated that it carried out 2,445 inspection tours to food facilities, 280 to pesticides and feed facilities, and 1,535 to pharmaceutical facilities and medical devices, in addition to routine visits and smart inspections.
| Publication Date |
2022-07-25
|
| Applying Date |
2022-07-25
|
