Philippines FDA registration MDR-09906

SMITH & NEPHEW FOOTPRINT ULTRA PK SUTURE ANCHOR

Name: SMITH & NEPHEW FOOTPRINT ULTRA PK SUTURE ANCHOR — Philippines FDA registration MDR-09906
Creator: Smith & Nephew Pte. Ltd.
Keywords: SMITH & NEPHEW FOOTPRINT ULTRA PK SUTURE ANCHOR, MDR-09906, Smith & Nephew Pte. Ltd., Endomed Trading, Inc., USA, Philippines FDA registration

PhilippinesSmith & Nephew Pte. Ltd.USAIssued July 02, 2020 – July 02, 2021

VerifiedFDA Philippines · official registry

Device information

Product Name: SMITH & NEPHEW FOOTPRINT ULTRA PK SUTURE ANCHOR
Registration Number: MDR-09906

Manufacturer details

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

Importer & distribution

Importer/Distributor: Endomed Trading, Inc.

Registration dates

Issuance Date: July 02, 2020
Expiry Date: July 02, 2021

About this record

Access comprehensive regulatory information for SMITH & NEPHEW FOOTPRINT ULTRA PK SUTURE ANCHOR in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-09906 and manufactured by Smith & Nephew Pte. Ltd. in USA. The device was registered on July 02, 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.