Philippines FDA registration MDR-01419
TERUMO™ TERUFLEX® BP-KIT (WITHOUT BLOOD TRANSFUSION FILTER)
Philippines·Terumo Corporation·Japan·Issued June 28, 2019 – August 01, 2024Device information
- Product Name
- TERUMO™ TERUFLEX® BP-KIT (WITHOUT BLOOD TRANSFUSION FILTER)
- Registration Number
- MDR-01419
Manufacturer details
- Manufacturer
- Terumo Corporation
- Country of Origin
- Japan
Importer & distribution
- Importer/Distributor
- Terumo Marketing Philippines, Inc.
Registration dates
- Issuance Date
- June 28, 2019
- Expiry Date
- August 01, 2024
About this record
Access comprehensive regulatory information for TERUMO™ TERUFLEX® BP-KIT (WITHOUT BLOOD TRANSFUSION FILTER) in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-01419 and manufactured by Terumo Corporation in Japan. The device was registered on June 28, 2019.
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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