International safety notice

Common names: (1) (2) Stationary digital general-purpose X-ray fluoroscopy diagnostic equipment (3) Stationary digital urinary/gynecological X-ray fluoroscopy diagnostic equipment device Sales name: (1) Luminos Session (2) Luminos Session Max (3) Uroscope Omnia Max

Japan / PMDA Recalls · JPN · Mar 1, 2023

Key facts

Regulator Japan / PMDA Recalls
Country JPN
Brand Common names: (1) (2) Stationary digital general-purpose X-ray fluoroscopy diagnostic equipment (3) Stationary digital urinary/gynecological X-ray fluoroscopy diagnostic equipment device Sales name: (1) Luminos Session (2) Luminos Session Max (3) Uroscope Omnia Max
Manufacturer Siemens Healthcare Co., Ltd.
Date Mar 1, 2023
Regulator page info.pmda.go.jp

At a glance

  • No Recall
  • No Field safety notice

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About International device safety notices

Field safety notices, recalls and safety alerts published by about 30 national medical device regulators outside the United States, matched by Orca1 to FDA device data.

Source: National medical device regulators (as listed), compiled by Orca1

Browse all International device safety notices