International safety notice

General name: (1),(2) Stationary digital circulatory system X-ray fluoroscopy diagnostic device (3) Ceiling-mounted X-ray tube support (4)X-ray tube support bed support table Brand name: (1) Angiography system Trinias (2) Angiography system BRANSIST safire (3) Ceiling traveling C-arm type holding device MH-200S (4) Cアーム type holding device for circulator MH-300

Japan / PMDA Recalls · JPN · Mar 14, 2024

Key facts

Regulator Japan / PMDA Recalls
Country JPN
Brand General name: (1),(2) Stationary digital circulatory system X-ray fluoroscopy diagnostic device (3) Ceiling-mounted X-ray tube support (4)X-ray tube support bed support table Brand name: (1) Angiography system Trinias (2) Angiography system BRANSIST safire (3) Ceiling traveling C-arm type holding device MH-200S (4) Cアーム type holding device for circulator MH-300
Manufacturer Shimadzu Corporation
Models 41F03C1C7001, 41EFFDD9B001, 41EFFDBD1001, 41EFFDB96001, 41EFFDBA1001, 41F003F99001, MH‐300, 41EFD4195001, 41EFFDBC7001, 41F0BF7D7002, 41F0D05D6001, 41EFFDB8A002 and 74 more
Date Mar 14, 2024
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

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