Philippines FDA registration MDR-05052B
POLAR SYSTEM LATERAL Ti/HA, NON-CEMENTED
Philippines·Smith & Nephew Pte. Limited·Switzerland·Issued January 23, 2020 – January 13, 2023Device information
- Product Name
- POLAR SYSTEM LATERAL Ti/HA, NON-CEMENTED
- Registration Number
- MDR-05052B
Manufacturer details
- Manufacturer
- Smith & Nephew Pte. Limited
- Country of Origin
- Switzerland
Importer & distribution
- Importer/Distributor
- RBGM Medical Express Sales, Inc.
Registration dates
- Issuance Date
- January 23, 2020
- Expiry Date
- January 13, 2023
About this record
Access comprehensive regulatory information for POLAR SYSTEM LATERAL Ti/HA, NON-CEMENTED in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-05052B and manufactured by Smith & Nephew Pte. Limited in Switzerland. The device was registered on January 23, 2020.
This page provides complete registration details including manufacturer information, importer/distributor details (RBGM Medical Express Sales, 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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