Philippines FDA registration MDR-01932

ARGYLE™ PEDIATRIC PERITONEAL DIALYSIS CATHETER TENCKHOFF, 2 CUFF

Philippines·Covidien Private Limited·USA·Issued July 24, 2020 – April 15, 2025

Device information

Product Name: ARGYLE™ PEDIATRIC PERITONEAL DIALYSIS CATHETER TENCKHOFF, 2 CUFF
Registration Number: MDR-01932

Manufacturer details

Manufacturer: Covidien Private Limited
Country of Origin: USA

Importer & distribution

Importer/Distributor: Medtronic Philippines, Inc.

Registration dates

Issuance Date: July 24, 2020
Expiry Date: April 15, 2025

About this record

Access comprehensive regulatory information for ARGYLE™ PEDIATRIC PERITONEAL DIALYSIS CATHETER TENCKHOFF, 2 CUFF in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-01932 and manufactured by Covidien Private Limited in USA. The device was registered on July 24, 2020.

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