Philippines FDA registration MDR-09977

PTFE ANGIOGRAPHIC GUIDEWIRE

Name: PTFE ANGIOGRAPHIC GUIDEWIRE — Philippines FDA registration MDR-09977
Creator: Medtronic International Ltd.
Keywords: PTFE ANGIOGRAPHIC GUIDEWIRE, MDR-09977, Medtronic International Ltd., Medtronic Philippines, Inc., USA, Philippines FDA registration

PhilippinesMedtronic International Ltd.USAIssued July 08, 2020 – July 08, 2021

VerifiedFDA Philippines · official registry

Device information

Product Name: PTFE ANGIOGRAPHIC GUIDEWIRE
Registration Number: MDR-09977

Manufacturer details

Manufacturer: Medtronic International Ltd.
Country of Origin: USA

Importer & distribution

Importer/Distributor: Medtronic Philippines, Inc.

Registration dates

Issuance Date: July 08, 2020
Expiry Date: July 08, 2021

About this record

Access comprehensive regulatory information for PTFE ANGIOGRAPHIC GUIDEWIRE in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-09977 and manufactured by Medtronic International Ltd. in USA. The device was registered on July 08, 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.