Murilo Freitas – Página 60

Monkeypox Update: FDA Takes Significant Action to Help Expand Access to Testing

Murilo Freitas - 20:39, 6 de septiembre de 2022404

Monkeypox Update: FDA Takes Significant Action to Help Expand Access to Testing
http://www.fda.gov/news-events/press-announcements/monkeypox-update-fda-takes-significant-action-help-expand-access-testing

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Certain Philips Respironics Masks for BiPAP, CPAP Machines Recalled Due to Safety Issue with Magnets That May Affect Certain Medical Devices

Murilo Freitas - 21:14, 5 de septiembre de 2022345

Certain Philips Respironics Masks for BiPAP, CPAP Machines Recalled Due to Safety Issue with Magnets That May Affect Certain Medical Devices
http://www.fda.gov/news-events/press-announcements/certain-philips-respironics-masks-bipap-cpap-machines-recalled-due-safety-issue-magnets-may-affect

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FDA Roundup: September 6, 2022

Murilo Freitas - 19:45, 5 de septiembre de 2022326

FDA Roundup: September 6, 2022
http://www.fda.gov/news-events/press-announcements/fda-roundup-september-6-2022

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Philips Respironics Alerts Customers Worldwide of Updated Instructions and Labeling of Specific Sleep Therapy Masks That Contain Magnetic Headgear Clips Due to Potential Risk of Serious Injury

Murilo Freitas - 04:00, 5 de septiembre de 2022355

Pittsburgh, Pennsylvania – Royal Philips’ (NYSE: PHG; AEX: PHIA) subsidiary Philips Respironics is alerting users of certain CPAP or Bi-Level PAP therapy masks with magnetic headgear clips or straps that these devices should not be used by or near patients and their household members, caregivers and

http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/philips-respironics-alerts-customers-worldwide-updated-instructions-and-labeling-specific-sleep

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FDA Roundup: September 2, 2022

Murilo Freitas - 17:45, 1 de septiembre de 2022417

FDA Roundup: September 2, 2022
http://www.fda.gov/news-events/press-announcements/fda-roundup-september-2-2022

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Moduladores y potenciadores para el tratamiento de personas con fibrosis quística con mutaciones Clase II (F508del) en el CFTR

Murilo Freitas - 00:00, 31 de agosto de 2022388

Moduladores y potenciadores para el tratamiento de personas con fibrosis quística con mutaciones Clase II (F508del) en el CFTR
https://sites.bvsalud.org/redetsa/brisa/resource/?id=biblioref.referencesource.1391934

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FDA Approves First Treatment for Acid Sphingomyelinase Deficiency, a Rare Genetic Disease

Murilo Freitas - 17:23, 30 de agosto de 2022335

FDA Approves First Treatment for Acid Sphingomyelinase Deficiency, a Rare Genetic Disease
http://www.fda.gov/news-events/press-announcements/fda-approves-first-treatment-acid-sphingomyelinase-deficiency-rare-genetic-disease

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Coronavirus (COVID-19) Update: FDA Authorizes Moderna, Pfizer-BioNTech Bivalent COVID-19 Vaccines for Use as a Booster Dose

Murilo Freitas - 13:42, 30 de agosto de 2022438

Coronavirus (COVID-19) Update: FDA Authorizes Moderna, Pfizer-BioNTech Bivalent COVID-19 Vaccines for Use as a Booster Dose
http://www.fda.gov/news-events/press-announcements/coronavirus-covid-19-update-fda-authorizes-moderna-pfizer-biontech-bivalent-covid-19-vaccines-use

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FDA Roundup: August 30, 2022

Murilo Freitas - 19:08, 29 de agosto de 2022317

FDA Roundup: August 30, 2022
http://www.fda.gov/news-events/press-announcements/fda-roundup-august-30-2022

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Hamilton Medical AG Recalls Hamilton-C6 Intensive Care Ventilator Due to Potential Water Ingress that May Cause Breathing Support to Stop

Murilo Freitas - 04:00, 28 de agosto de 2022379

If water enters the Hamilton-C6 Intensive Care Ventilator due to a loose status indicator board, it may cause the ventilator to stop providing breathing support.

http://www.fda.gov/medical-devices/medical-device-recalls/hamilton-medical-ag-recalls-hamilton-c6-intensive-care-ventilator-due-potential-water-ingress-may