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EDWARDS LIFESCIENCES CARPENTIER-EDWARD PERIMOUNT MAGNA EASR PERICARDIAL BIOPROSTHESIS (MITRAL) - FDA Registration MDR-04855

Access comprehensive regulatory information for EDWARDS LIFESCIENCES CARPENTIER-EDWARD PERIMOUNT MAGNA EASR PERICARDIAL BIOPROSTHESIS (MITRAL) in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-04855 and manufactured by Edward Lifesciences LLC One Edwards Way, Irvine, CA 92614, United States of America in USA. The device was registered on May 14, 2024.

This page provides complete registration details including manufacturer information, importer/distributor details (R.G. Meditron, 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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MDR-04855
EDWARDS LIFESCIENCES CARPENTIER-EDWARD PERIMOUNT MAGNA EASR PERICARDIAL BIOPROSTHESIS (MITRAL)
Registered medical device in Philippines
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Device Information
Product Name
EDWARDS LIFESCIENCES CARPENTIER-EDWARD PERIMOUNT MAGNA EASR PERICARDIAL BIOPROSTHESIS (MITRAL)
Registration Number
MDR-04855
Importer & Distribution
Importer/Distributor
R.G. Meditron, Inc.
Registration Dates
Issuance Date
May 14, 2024
Expiry Date
October 19, 2027