Pure Global

"Termo" Akufoss coronary balloon dilation catheter - Taiwan Registration d1272115be69ccf87c007b752528fd1d

Access comprehensive regulatory information for "Termo" Akufoss coronary balloon dilation catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number d1272115be69ccf87c007b752528fd1d and manufactured by TERUMO CORPORATION;; ASHITAKA FACTORY OF TERUMO CORPORATION. The authorized representative in Taiwan is TERUMO TAIWAN MEDICAL CO., LTD..

This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

Free Database
Powered by Pure Global AI
89,000+ Devices
d1272115be69ccf87c007b752528fd1d
Registration Details
Taiwan FDA Registration: d1272115be69ccf87c007b752528fd1d
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

"Termo" Akufoss coronary balloon dilation catheter
TW: โ€œๆณฐ็ˆพ่Œ‚โ€้˜ฟ้…ทไฝ›ๆ–ฏๅ† ็‹€ๅ‹•่„ˆๆฑฝ็ƒๆ“ดๅผตๅฐŽ็ฎก
Risk Class 3

Registration Details

d1272115be69ccf87c007b752528fd1d

DHA05602940905

Company Information

Product Details

For details, it is Chinese approved copy of the imitation order

E Cardiovascular Medicine Science

E.0005.

import

Dates and Status

Mar 13, 2017

Mar 13, 2027