Philippines FDA registration MDR-10921

ULTRA FAST-FIX ASSEMBLY Y-CURVED

Philippines·Smith & Nephew Endoscopy - Singapore mfd. By: Arthrocare Corporation - TX, USA For: Endoscopy Smith & Nephew, Inc. - Andover, MA, USA·USA·Issued June 03, 2021 – June 03, 2022

Device information

Product Name: ULTRA FAST-FIX ASSEMBLY Y-CURVED
Registration Number: MDR-10921

Manufacturer details

Manufacturer: Smith & Nephew Endoscopy - Singapore mfd. By: Arthrocare Corporation - TX, USA For: Endoscopy Smith & Nephew, Inc. - Andover, MA, USA
Country of Origin: USA

Importer & distribution

Importer/Distributor: Endomed Trading, Inc.

Registration dates

Issuance Date: June 03, 2021
Expiry Date: June 03, 2022

About this record

Access comprehensive regulatory information for ULTRA FAST-FIX ASSEMBLY Y-CURVED in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-10921 and manufactured by Smith & Nephew Endoscopy - Singapore mfd. By: Arthrocare Corporation - TX, USA For: Endoscopy Smith & Nephew, Inc. - Andover, MA, USA in USA. The device was registered on June 03, 2021.

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.