Philippines FDA registration DVR-5037
TERUMO RADIFOCUS OPTITORQUE ANGIOGRAPHIC CATHETER
Philippines·Terumo Corporation·Japan·Issued August 13, 2020 – March 23, 2025Device information
- Product Name
- TERUMO RADIFOCUS OPTITORQUE ANGIOGRAPHIC CATHETER
- Registration Number
- DVR-5037
Manufacturer details
- Manufacturer
- Terumo Corporation
- Country of Origin
- Japan
Importer & distribution
- Importer/Distributor
- Terumo Marketing Philippines, Inc.
Registration dates
- Issuance Date
- August 13, 2020
- Expiry Date
- March 23, 2025
About this record
Access comprehensive regulatory information for TERUMO RADIFOCUS OPTITORQUE ANGIOGRAPHIC CATHETER in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number DVR-5037 and manufactured by Terumo Corporation in Japan. The device was registered on August 13, 2020.
This page provides complete registration details including manufacturer information, importer/distributor details (Terumo Marketing 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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