Devices

Device Recall Bulk Microsurgical Knife 1.2mm Sideport Knife

Model / Serial
Lot No.: DK0207Q, DK0307I, DK0407M, DK0507R
Product Classification
Ophthalmic Devices
Device Class
1
Implanted device?
No
Distribution
Worldwide: USA, Kuwait, Lebanon, Lithuania, Mexico, Netherlands, Norway, South Africa, Saudi Arabia, Slovakia, Spain, Sweden, Switzwerland, Turkey, United Kingdom, Ecuador, Finland, France, Germany, Greece, Italy, Denmark, Columbia, Chile, Brazil, Belgium, and Australia
Product Description
Premier Edge, Bulk Microsurgical Knife. 1.2mm, Sideport Knife, Item Code B-PE3012, Oasis, Gendora, CA
Manufacturer
Oasis Medical Inc
1 Event
- Recall of Device Recall Bulk Microsurgical Knife 1.2mm Sideport Knife

Manufacturer

Oasis Medical Inc

Manufacturer Address
Oasis Medical Inc, 514 S Vermont Ave Bldg 510-528, Glendora CA 91741-6205
Manufacturer Parent Company (2017)
Oasis Medical Inc.
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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