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EAGLE EYE PLATINUM RX DIGITAL IVUS CATHETER - FDA Registration MDR-03239

Access comprehensive regulatory information for EAGLE EYE PLATINUM RX DIGITAL IVUS CATHETER in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-03239 and manufactured by Volcano Corporation in USA. The device was registered on August 31, 2016.

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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USA
MDR-03239
EAGLE EYE PLATINUM RX DIGITAL IVUS CATHETER
Registered medical device in Philippines
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Device Information
Product Name
EAGLE EYE PLATINUM RX DIGITAL IVUS CATHETER
Registration Number
MDR-03239
Manufacturer Details
Country of Origin
USA
Importer & Distribution
Importer/Distributor
R.G. Meditron, Inc.
Registration Dates
Issuance Date
August 31, 2016
Expiry Date
July 06, 2021