Philippines FDA registration MDR-04918
TERUMO® CATHELIN NEEDLE®
Device information
- Product Name
- TERUMO® CATHELIN NEEDLE®
- Registration Number
- MDR-04918
Manufacturer details
- Manufacturer
- Terumo (Philippines) Corporation
- Country of Origin
- Philippines
Importer & distribution
- Importer/Distributor
- Terumo (Philippines) Corporation
Registration dates
- Issuance Date
- January 22, 2020
- Expiry Date
- November 17, 2022
About this record
Access comprehensive regulatory information for TERUMO® CATHELIN NEEDLE® in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-04918 and manufactured by Terumo (Philippines) Corporation in Philippines. The device was registered on January 22, 2020.
This page provides complete registration details including manufacturer information, importer/distributor details (Terumo (Philippines) Corporation), 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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