Philippines FDA registration MDR-01551

SV .018’’ STEERABLE GUIDEWIRES

Philippines flagPhilippines·Cordis Corporation- 14201 North West 60th Avenue, Miami Lakes, Florida, 33014, USA Mfd by: Lake Region Medical Ltd.- Butlersland New Ross Co. Wexford Ireland·Ireland·Issued March 05, 2025 – October 09, 2029
Device information
Product Name
SV .018’’ STEERABLE GUIDEWIRES
Registration Number
MDR-01551
Manufacturer details
Country of Origin
Ireland
Importer & distribution
Importer/Distributor
Getz Bros. Philippines, Inc.
Registration dates
Issuance Date
March 05, 2025
Expiry Date
October 09, 2029
About this record

Access comprehensive regulatory information for SV .018’’ STEERABLE GUIDEWIRES in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-01551 and manufactured by Cordis Corporation- 14201 North West 60th Avenue, Miami Lakes, Florida, 33014, USA Mfd by: Lake Region Medical Ltd.- Butlersland New Ross Co. Wexford Ireland in Ireland. The device was registered on March 05, 2025.

This page provides complete registration details including manufacturer information, importer/distributor details (Getz Bros. Philippines, 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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