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IMPLANT CAST TOTAL HIP REPLACEMENT ARTHROPLASTY, BIOLOX DELTA CUP INSERT, CERAMIC - FDA Registration MDR-08631I

Access comprehensive regulatory information for IMPLANT CAST TOTAL HIP REPLACEMENT ARTHROPLASTY, BIOLOX DELTA CUP INSERT, CERAMIC in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-08631I and manufactured by Implantcast GmbH in Germany. The device was registered on March 03, 2020.

This page provides complete registration details including manufacturer information, importer/distributor details (Ilix Medical Implant Trading, 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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Germany
MDR-08631I
IMPLANT CAST TOTAL HIP REPLACEMENT ARTHROPLASTY, BIOLOX DELTA CUP INSERT, CERAMIC
Registered medical device in Philippines
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Device Information
Product Name
IMPLANT CAST TOTAL HIP REPLACEMENT ARTHROPLASTY, BIOLOX DELTA CUP INSERT, CERAMIC
Registration Number
MDR-08631I
Manufacturer Details
Manufacturer
Implantcast GmbH
Country of Origin
Germany
Importer & Distribution
Registration Dates
Issuance Date
March 03, 2020
Expiry Date
March 03, 2021