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IMPLANT CAST TOTAL KNEE REPLACEMENT ARTHROPLASTY, ACS® MB SC TIBIAL SPACER II/MM - FDA Registration MDR-09140Q

Access comprehensive regulatory information for IMPLANT CAST TOTAL KNEE REPLACEMENT ARTHROPLASTY, ACS® MB SC TIBIAL SPACER II/MM in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-09140Q and manufactured by Implantcast GmbH in Germany. The device was registered on January 15, 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-09140Q
IMPLANT CAST TOTAL KNEE REPLACEMENT ARTHROPLASTY, ACS® MB SC TIBIAL SPACER II/MM
Registered medical device in Philippines
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Device Information
Product Name
IMPLANT CAST TOTAL KNEE REPLACEMENT ARTHROPLASTY, ACS® MB SC TIBIAL SPACER II/MM
Registration Number
MDR-09140Q
Manufacturer Details
Manufacturer
Implantcast GmbH
Country of Origin
Germany
Importer & Distribution
Registration Dates
Issuance Date
January 15, 2020
Expiry Date
January 15, 2021