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RELIANCE 4-FRONT IMPLANTABLE DEFIBRILLATOR LEAD DUAL COIL, PASSIVE FIX, IROX-COATED ELECTRODE WITH SILICONE - FDA Registration MDR-08051D

Access comprehensive regulatory information for RELIANCE 4-FRONT IMPLANTABLE DEFIBRILLATOR LEAD DUAL COIL, PASSIVE FIX, IROX-COATED ELECTRODE WITH SILICONE in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-08051D and manufactured by Cardiac Pacemakers Inc. (Boston Scientific Corporation) in Ireland. The device was registered on March 18, 2020.

This page provides complete registration details including manufacturer information, importer/distributor details (Boston Scientific 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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Ireland
MDR-08051D
RELIANCE 4-FRONT IMPLANTABLE DEFIBRILLATOR LEAD DUAL COIL, PASSIVE FIX, IROX-COATED ELECTRODE WITH SILICONE
Registered medical device in Philippines
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Device Information
Product Name
RELIANCE 4-FRONT IMPLANTABLE DEFIBRILLATOR LEAD DUAL COIL, PASSIVE FIX, IROX-COATED ELECTRODE WITH SILICONE
Registration Number
MDR-08051D
Manufacturer Details
Importer & Distribution
Importer/Distributor
Boston Scientific Phils., Inc.
Registration Dates
Issuance Date
March 18, 2020
Expiry Date
April 25, 2025