Devices

Device Recall Fujifilm Endoscope; ED530XT

Model / Serial
All distribution dates :3/2003-4/2016
Product Classification
Gastroenterology-Urology Devices
Device Class
2
Implanted device?
No
Distribution
Nationwide Distribution.
Product Description
Endoscope; ED-530XT Operation Manual || 'Operation and Preparation' and 'Cleaning, Disinfection and Storage'
Manufacturer
Fujifilm Medical Systems U.S.A., Inc.
1 Event
- Recall of Device Recall Fujifilm Endoscope; ED530XT

Manufacturer

Fujifilm Medical Systems U.S.A., Inc.

Manufacturer Address
Fujifilm Medical Systems U.S.A., Inc., 10 Highpoint Dr, Wayne NJ 07470-7431
Manufacturer Parent Company (2017)
FUJIFILM Holdings Corp.
Source
USFDA

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Medical devices help to diagnose, prevent and treat many injuries and diseases. We are not suggesting or implying that any companies or other entities included in the International Medical Devices Database engaged in unlawful conduct or otherwise acted improperly. The same device may have different names in different countries. This database is not intended to provide medical advice and patients should check with their doctors to determine if it contains relevant information and if such information has medical implications for them.

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