Philippines FDA registration MDR-08114

ARROW-CLARK™ VECTORFLOW™ RETROGRADE HEMODIALYSIS CATHETERIZATION SET

Philippines flagPhilippines·Teleflex Medical·USA·Issued April 01, 2020 – May 09, 2025
Device information
Product Name
ARROW-CLARK™ VECTORFLOW™ RETROGRADE HEMODIALYSIS CATHETERIZATION SET
Registration Number
MDR-08114
Manufacturer details
Manufacturer
Teleflex Medical
Country of Origin
USA
Importer & distribution
Registration dates
Issuance Date
April 01, 2020
Expiry Date
May 09, 2025
About this record

Access comprehensive regulatory information for ARROW-CLARK™ VECTORFLOW™ RETROGRADE HEMODIALYSIS CATHETERIZATION SET in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-08114 and manufactured by Teleflex Medical in USA. The device was registered on April 01, 2020.

This page provides complete registration details including manufacturer information, importer/distributor details (IDS Medical Systems 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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