Philippines FDA registration MDR-01543

BIOSURE HA INTERFERENCE SCREW

Name: BIOSURE HA INTERFERENCE SCREW — Philippines FDA registration MDR-01543
Creator: Smith & Nephew Pte. Limited
Keywords: BIOSURE HA INTERFERENCE SCREW, MDR-01543, Smith & Nephew Pte. Limited, Endomed Trading Inc., USA, Philippines FDA registration

PhilippinesSmith & Nephew Pte. LimitedUSAIssued January 21, 2020 – October 02, 2024

VerifiedFDA Philippines · official registry

Device information

Product Name: BIOSURE HA INTERFERENCE SCREW
Registration Number: MDR-01543

Manufacturer details

Manufacturer: Smith & Nephew Pte. Limited
Country of Origin: USA

Importer & distribution

Importer/Distributor: Endomed Trading Inc.

Registration dates

Issuance Date: January 21, 2020
Expiry Date: October 02, 2024

About this record

Access comprehensive regulatory information for BIOSURE HA INTERFERENCE SCREW in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-01543 and manufactured by Smith & Nephew Pte. Limited in USA. The device was registered on January 21, 2020.

This page provides complete registration details including manufacturer information, importer/distributor details (Endomed 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.