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ENDURITY™ CORE PACEMAKER - FDA Registration MDR-08173A

Access comprehensive regulatory information for ENDURITY™ CORE PACEMAKER in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-08173A and manufactured by Abbott Medical (Singapore) Pte. Ltd. in Puerto Rico. The device was registered on April 01, 2020.

This page provides complete registration details including manufacturer information, importer/distributor details (Biodevices 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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Puerto Rico
MDR-08173A
ENDURITY™ CORE PACEMAKER
Registered medical device in Philippines
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Device Information
Product Name
ENDURITY™ CORE PACEMAKER
Registration Number
MDR-08173A
Manufacturer Details
Country of Origin
Puerto Rico
Importer & Distribution
Importer/Distributor
Biodevices Inc.
Registration Dates
Issuance Date
April 01, 2020
Expiry Date
May 27, 2025