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PARCUS® TITANIUM INTERFERENCE SCREW - FDA Registration MDR-06279

Access comprehensive regulatory information for PARCUS® TITANIUM INTERFERENCE SCREW in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-06279 and manufactured by Parcus Medical, LLC 6423 Parkland Drive, Sarasota, Florida 34243 USA in USA. The device was registered on February 07, 2024.

This page provides complete registration details including manufacturer information, importer/distributor details (Bone Fix Metal Craft), 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-06279
PARCUS® TITANIUM INTERFERENCE SCREW
Registered medical device in Philippines
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Device Information
Product Name
PARCUS® TITANIUM INTERFERENCE SCREW
Registration Number
MDR-06279
Manufacturer Details
Importer & Distribution
Importer/Distributor
Bone Fix Metal Craft
Registration Dates
Issuance Date
February 07, 2024
Expiry Date
December 01, 2028