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DTSTART;TZID=Asia/Tokyo:20260430T000000
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PRIORITY:5
TRANSP:OPAQUE
SUMMARY:米国｜FDA、放射線治療用マーキングデバイスなどをクラスII（特別管理）に分類する最終規則
DESCRIPTION:\nMedical Devices; Cardiovascular Devices; Classification of the Laser-Powered Inferior Vena Cava Filter Retrieval Catheter ( https://www.federalregister.gov/documents/2026/04/30/2026-08426/medical-devices-cardiovascular-devices-classification-of-the-laser-powered-inferior-vena-cava-filter )\n\n\n\nMedical Devices; Radiology Devices; Classification of the Radiation Therapy Marking Device ( https://www.federalregister.gov/documents/2026/04/30/2026-08424/medical-devices-radiology-devices-classification-of-the-radiation-therapy-marking-device )\n\n\n\nMedical Devices; Neurological Devices; Classification of the Brain Temperature Measurement System ( https://www.federalregister.gov/documents/2026/04/30/2026-08425/medical-devices-neurological-devices-classification-of-the-brain-temperature-measurement-system )\n
URL:https://compliance-calendar.sakiyomi.co.jp/events/%e7%b1%b3%e5%9b%bd%ef%bd%9cfda%e3%80%81%e6%94%be%e5%b0%84%e7%b7%9a%e6%b2%bb%e7%99%82%e7%94%a8%e3%83%9e%e3%83%bc%e3%82%ad%e3%83%b3%e3%82%b0%e3%83%87%e3%83%90%e3%82%a4%e3%82%b9%e3%81%aa%e3%81%a9/
CATEGORIES:セクター,医療・医薬品,注目領域,製品認証・適合性評価
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