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BARD® FLUORO-4™ SILICONE URETERAL COIL STENT - FDA Registration DVR-6393

Access comprehensive regulatory information for BARD® FLUORO-4™ SILICONE URETERAL COIL STENT in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number DVR-6393 and manufactured by Bard Shannon Ltd. in USA. The device was registered on March 14, 2019.

This page provides complete registration details including manufacturer information, importer/distributor details (Healthsolutions Enterprises Inc.), and regulatory compliance data from the official Philippines FDA medical device database. Pure Global AI offers free access to Philippines' complete medical device registry, helping global MedTech companies navigate FDA regulations efficiently.

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USA
DVR-6393
BARD® FLUORO-4™ SILICONE URETERAL COIL STENT
Registered medical device in Philippines
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Device Information
Product Name
BARD® FLUORO-4™ SILICONE URETERAL COIL STENT
Registration Number
DVR-6393
Manufacturer Details
Manufacturer
Bard Shannon Ltd.
Country of Origin
USA
Importer & Distribution
Registration Dates
Issuance Date
March 14, 2019
Expiry Date
January 22, 2024