AMPLATZER™ GUIDEWIRE FIXED, NOODLE WIRE - FDA Registration DVR-6286
Access comprehensive regulatory information for AMPLATZER™ GUIDEWIRE FIXED, NOODLE WIRE in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number DVR-6286 and manufactured by St. Jude Medical (Singapore) Pte. Ltd. in USA. The device was registered on December 06, 2018.
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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USA
DVR-6286
AMPLATZER™ GUIDEWIRE FIXED, NOODLE WIRE
Registered medical device in Philippines
Device Information
Product Name
AMPLATZER™ GUIDEWIRE FIXED, NOODLE WIRE
Registration Number
DVR-6286
Manufacturer Details
Manufacturer
St. Jude Medical (Singapore) Pte. Ltd.Country of Origin
USA
Importer & Distribution
Importer/Distributor
Biodevices Inc.Registration Dates
Issuance Date
December 06, 2018
Expiry Date
November 09, 2023

