Devices

FiberOptix Ultra 8 IAB@ 8Fr 30cc,Ultra IAB: 8Fr 30cc, FiberOptix Ultra 8 IAB@ 8Fr 40cc, Ultra IAB: 8Fr 40cc, Ultra Flex IAB: 7.5Fr 30cc, Ultra Flex IAB: 7.5Fr 35cc, Ultra Flex IAB: 7.5Fr 40cc, RediGuard IAB: 7Fr 30cc

Model / Serial
Product Classification
Cardiovascular Devices
Product Description
Arrow International: FiberOptix Ultra 8 IAB@ 8Fr 30cc,Ultra IAB: 8Fr 30cc, FiberOptix Ultra 8 IAB@ 8Fr 40cc, Ultra IAB: 8Fr 40cc, Ultra Flex IAB: 7.5Fr 30cc, Ultra Flex IAB: 7.5Fr 35cc, Ultra Flex IAB: 7.5Fr 40cc, RediGuard IAB: 7Fr 30cc
Manufacturer
Arrow International
1 Event
- Safety Alert Or Field Safety Notices for FiberOptix Ultra 8 IAB@ 8Fr 30cc,Ultra IAB: 8Fr 30cc, FiberOptix Ultra 8 IAB@ 8Fr 40cc, Ultra IAB: 8Fr 40cc, Ultra Flex IAB: 7.5Fr 30cc, Ultra Flex IAB: 7.5Fr 35cc, Ultra Flex IAB: 7.5Fr 40cc, RediGuard IAB: 7Fr 30cc

Manufacturer

Arrow International

Manufacturer Parent Company (2017)
Teleflex Incorporated
Source
MHRA

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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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