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WEBSTER®ELECTROPHYSIOLOGY CATHETER - FDA Registration DVR-7762

Access comprehensive regulatory information for WEBSTER®ELECTROPHYSIOLOGY CATHETER in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number DVR-7762 and manufactured by Biosense Webster, Inc. - 31 Technology Drive, Irvine, California 92618, USA mfd. by: Biosense Webster, Inc. Circuito Interior Norte 1820, Parque Industrial Salvarcar, Cuidad Juarez, Chihuahua 32574, Mexico in Mexico. The device was registered on May 22, 2025.

This page provides complete registration details including manufacturer information, importer/distributor details (Johnson & Johnson (Philippines), 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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DVR-7762
WEBSTER®ELECTROPHYSIOLOGY CATHETER
Registered medical device in Philippines
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Device Information
Product Name
WEBSTER®ELECTROPHYSIOLOGY CATHETER
Registration Number
DVR-7762
Importer & Distribution
Registration Dates
Issuance Date
May 22, 2025
Expiry Date
April 15, 2031