菲律宾

SOMNOMED INC. 在FDA注册了两款PLC代码的产品。

Terumo（菲律宾）公司已注册产品代码FMF的医疗器械。

FDA解除对未通知医疗器械的公共健康警告。

FDA警告不要使用未通知的医疗器械“PRIME BROWN™弹性绷带REF.BB10”。

FDA警告购买假冒Ulthera®系统，强调医疗设备的公共健康风险。

FDA警告购买未注册的医疗设备，影响北美及其他地区的安全。

FDA PH Advisory: Lifting of the FDA Advisory No. 2021-1678 entitled “Public Health Warning Against the Purchase and Use of the Unnotified Medical Device Product Long Bone Plaster of Paris Bandage (6” x 5y )” - fda.gov.ph

FDA PH Advisory: FDA Advisory No.2023-0364 || Public Health Warning Against the Purchase and Use of Counterfeit Medical Device “Ulthera® System” - Food and Drug Administration - fda.gov.ph

LeMaitre将参加Needham虚拟医疗科技与诊断会议，强调行业参与。

FDA PH Advisory: FDA Advisory No.2026-0675 || Public Health Warning Against the Purchase and Use of the Medical Device Product “HEXACARE DISPOSABLE INFUSION SET NON-PYROGENIC, NON-TOXIC, ADULT” with Expired Certificate of Product Registration (CPR) - fda.gov.ph

FDA PH Advisory: FDA Advisory No.2024-1105 || Public Health Warning Against the Purchase and Use of the Unnotified Medical Device Product “BERKLEY JENSEN® BANDAGES” - Food and Drug Administration - fda.gov.ph

FDA PH Advisory: Lifting of the FDA Advisory No. 2023-1596 entitled “Public Health Warning Against the Purchase and Use of the Unnotified Medical Device Product “R&R REXI CARE ICE/HOT BAG”” - fda.gov.ph