Philippines FDA registration MDR-05052B

POLAR SYSTEM LATERAL Ti/HA, NON-CEMENTED

Name: POLAR SYSTEM LATERAL Ti/HA, NON-CEMENTED — Philippines FDA registration MDR-05052B
Creator: Smith & Nephew Pte. Limited
Keywords: POLAR SYSTEM LATERAL Ti/HA, NON-CEMENTED, MDR-05052B, Smith & Nephew Pte. Limited, RBGM Medical Express Sales, Inc., Switzerland, Philippines FDA registration

PhilippinesSmith & Nephew Pte. LimitedSwitzerlandIssued January 23, 2020 – January 13, 2023

VerifiedFDA Philippines · official registry

Device 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.