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SUPERA PERIPHERAL STENT SYSTEM - FDA Registration MDR-09639

Access comprehensive regulatory information for SUPERA PERIPHERAL STENT SYSTEM in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-09639 and manufactured by Abbott Vascular in USA. The device was registered on April 27, 2020.

This page provides complete registration details including manufacturer information, importer/distributor details (Abbott Laboratories), 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-09639
SUPERA PERIPHERAL STENT SYSTEM
Registered medical device in Philippines
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Device Information
Product Name
SUPERA PERIPHERAL STENT SYSTEM
Registration Number
MDR-09639
Manufacturer Details
Manufacturer
Abbott Vascular
Country of Origin
USA
Importer & Distribution
Importer/Distributor
Abbott Laboratories
Registration Dates
Issuance Date
April 27, 2020
Expiry Date
April 27, 2021