ANGIO CATHETER 3 CORONARY ANGIOGRAPHY (CAG) CATHETER STERILIZED PRODUCT (TYPE A) - JL FORMING TYPE
Philippines·Toyoflex Cebu Corporation - Lot 14, Block 2, Cebu Light Industrial Park (CLIP), Basak, Lapu-Lapu, Cebu·Philippines·Issued January 13, 2021 – January 13, 2022- Product Name
- ANGIO CATHETER 3 CORONARY ANGIOGRAPHY (CAG) CATHETER STERILIZED PRODUCT (TYPE A) - JL FORMING TYPE
- Registration Number
- MDR-10628A
- Manufacturer
- Toyoflex Cebu Corporation - Lot 14, Block 2, Cebu Light Industrial Park (CLIP), Basak, Lapu-Lapu, Cebu
- Country of Origin
- Philippines
- Importer/Distributor
- Toyoflex Cebu Corporation
- Issuance Date
- January 13, 2021
- Expiry Date
- January 13, 2022
Access comprehensive regulatory information for ANGIO CATHETER 3 CORONARY ANGIOGRAPHY (CAG) CATHETER STERILIZED PRODUCT (TYPE A) - JL FORMING TYPE in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-10628A and manufactured by Toyoflex Cebu Corporation - Lot 14, Block 2, Cebu Light Industrial Park (CLIP), Basak, Lapu-Lapu, Cebu in Philippines. The device was registered on January 13, 2021.
This page provides complete registration details including manufacturer information, importer/distributor details (Toyoflex Cebu 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.