Myanmar FDA registration 8183f1ef81b67e8615bda7f320497b91

Angiographic Catheter (RADIFOCUS GLIDECATH)

Myanmar·TERUMO·Ashitaka Factory of Terumo Corporation·Registered November 10, 2021

Device classification

Brand Name: TERUMO

Registration information

Analysis ID: 8183f1ef81b67e8615bda7f320497b91
Registration Date: November 10, 2021

Manufacturer

Name: Ashitaka Factory of Terumo Corporation

Authorized Representative

Name: NI LAY NAING COMPANY LIMITED

About this record

Access comprehensive regulatory information for Angiographic Catheter (RADIFOCUS GLIDECATH) in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 8183f1ef81b67e8615bda7f320497b91 and manufactured by Ashitaka Factory of Terumo Corporation. The device was registered on November 10, 2021.

This page provides complete registration details including manufacturer information, authorized representative details, and regulatory compliance data from the official Myanmar FDA medical device database. Pure Global AI offers free access to Myanmar's complete medical device registry.