- Role
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EUDAMED update: Feb 19, 2026
JP-MF-000010401JP-MF-0000104015 EU importers place this manufacturer's devices
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SRN
An SRN is the unique EUDAMED identifier assigned to a manufacturer, authorised representative or importer when it registers as an actor.
View in glossary →SRN
An SRN is the unique EUDAMED identifier assigned to a manufacturer, authorised representative or importer when it registers as an actor.
View in glossary →Devices placed in 31 countries
FUJIFILM Corporation is a medical device manufacturer registered in EUDAMED. The company has 505 devices on the EU market across 31 countries. It holds 2 valid CE certificates. Headquartered in Tokyo, Japan. Explore the regulatory profile, devices and certificates on MD Atlas.
Showing 1–25 of 176 device families.
457359621C23RV/C23Q4457359621C2519K457359621C41VBR457359621C2529M457359621L64LF457359621C2539P457359621MXS1L9457359621C253A46457359621C25PBF457359621C41V168457359621C35JT457359621C41BAH457359621C41L47RPA6457359621C4219L457359621L43LAP8K457359621CC41R8D457359621MXS2ESLL1WN457359621CC41R25N457359621R41RES457359621S11LV457359621CL4416R1CZ457359621S121CM457359621S211CP457359621S31M3457359621L34L6Certificate 4203162CE01Rev. 1Manufacturer
FUJIFILM Corporation
Notified body
DEKRA Certification B.V.
0344Version
1
Valid from
7/15/2024
Valid until
6/27/2029
Certificate HZ 1194536-1Rev. Rev.13Manufacturer
FUJIFILM Corporation
Notified body
TÜV Rheinland LGA Products GmbH
0197Version
3
Valid from
12/24/2025
Valid until
9/28/2026
Certificate HZ 1194536-2Rev. 1Manufacturer
FUJIFILM Corporation
Notified body
TÜV Rheinland LGA Products GmbH
0197Version
1
Valid from
7/13/2026
Valid until
7/12/2031
Certificate HZ 1194536-2Rev. Rev.0Manufacturer
FUJIFILM Corporation
Notified body
TÜV Rheinland LGA Products GmbH
0197Version
1
Valid from
12/24/2025
Valid until
7/12/2026
Showing 1–25 of 505 devices.