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PROXIMATE® PROCEDURE FOR PROLAPSE AND HEMORRHOIDS (PPH) SET - FDA Registration DVR-4595

Access comprehensive regulatory information for PROXIMATE® PROCEDURE FOR PROLAPSE AND HEMORRHOIDS (PPH) SET in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number DVR-4595 and manufactured by Ethicon Endo-Surgery, LLC in Mexico. The device was registered on September 06, 2019.

This page provides complete registration details including manufacturer information, importer/distributor details (Johnson & Johnson (Phils.) 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-4595
PROXIMATE® PROCEDURE FOR PROLAPSE AND HEMORRHOIDS (PPH) SET
Registered medical device in Philippines
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Device Information
Product Name
PROXIMATE® PROCEDURE FOR PROLAPSE AND HEMORRHOIDS (PPH) SET
Registration Number
DVR-4595
Manufacturer Details
Country of Origin
Mexico
Importer & Distribution
Registration Dates
Issuance Date
September 06, 2019
Expiry Date
October 28, 2024