ARGYLE™ PEDIATRIC PERITONEAL DIALYSIS CATHETER TENCKHOFF, 2 CUFF - FDA Registration MDR-01932
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.
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USA
MDR-01932
ARGYLE™ PEDIATRIC PERITONEAL DIALYSIS CATHETER TENCKHOFF, 2 CUFF
Registered medical device in Philippines
Device Information
Product Name
ARGYLE™ PEDIATRIC PERITONEAL DIALYSIS CATHETER TENCKHOFF, 2 CUFF
Registration Number
MDR-01932
Manufacturer Details
Manufacturer
Covidien Private LimitedCountry of Origin
USA
Importer & Distribution
Importer/Distributor
Medtronic Philippines, Inc.Registration Dates
Issuance Date
July 24, 2020
Expiry Date
April 15, 2025

