Philippines FDA registration MDR-10774

UNITE CORONARY ANGIOGRAPHY (CAG) CATHETER STERILIZED PRODUCT (TYPE A)

Philippines flagPhilippines·Toyoflex Cebu Corporation - Lot 14, Block 2, Cebu Light Industrial Park (CLIP), Basak, Lapu-Lapu, Cebu·Philippines·Issued January 13, 2021 – January 13, 2022
Device information
Product Name
UNITE CORONARY ANGIOGRAPHY (CAG) CATHETER STERILIZED PRODUCT (TYPE A)
Registration Number
MDR-10774
Manufacturer details
Country of Origin
Philippines
Importer & distribution
Importer/Distributor
Toyoflex Cebu Corporation
Registration dates
Issuance Date
January 13, 2021
Expiry Date
January 13, 2022
About this record

Access comprehensive regulatory information for UNITE CORONARY ANGIOGRAPHY (CAG) CATHETER STERILIZED PRODUCT (TYPE A) in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-10774 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.

Free DatabasePowered by Pure Global AIFDA Official DataPhilippines