53. • When fully implemented, the label of most devices
will include a unique device identifier (UDI) in
human- and machine-readable form, which will
ultimately improve patient safety, modernize device
postmarket surveillance, and facilitate medical
device innovation.
53
https://www.fda.gov/medical-devices/device-advice-comprehensive-regulatory-
assistance/unique-device-identification-system-udi-system
人および機械で認識可能な形式のunique device identifier (UDI)
最終的には患者の安全性を向上させ、デバイスの市販後調査を
近代化し、医療機器のイノベーションを促進することができる