Devices

Device Recall Hydrophilic Wire

Model / Serial
All lot codes.
Product Classification
Cardiovascular Devices
Device Class
2
Implanted device?
No
Distribution
Worldwide Distribution -- US including Puerto Rico and states of AL, CA, CO, FL, GA, IL, KS, LA, MA, MI, MN, MO, MT, NC, NJ, NV, NY, PA, SC, TN, TX, UT, VA and WI and countries of Germany, Thailand, Turkey and the Netherlands.
Product Description
Hydrophilic Guidewire, Catalog Number: VM18352, .035/150 cm, regular/angled/standard, sold as a single hydrophilic guidewire in sterile packaging. VisioMed International Group Inc., 14555 South Robert Trail - #208, Rosemount, MN 55068, www.visiomedical.com.
Manufacturer
Argon Medical Devices, Inc
2 Events
- Recall of Device Recall Hydrophilic Wire
- Recall of Device Recall Hydrophilic Wire

Manufacturer

Argon Medical Devices, Inc

Manufacturer Address
Argon Medical Devices, Inc, 1445 Flat Creek Rd, Athens TX 75751
Manufacturer Parent Company (2017)
RoundTable Healthcare Partners Lp
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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