Pure Global

"Belsen" Kema coronary stent system - Taiwan Registration 7727c9dacb469f3f4b564422270f03ea

Access comprehensive regulatory information for "Belsen" Kema coronary stent system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 7727c9dacb469f3f4b564422270f03ea and manufactured by BIOSENSORS EUROPE SA;; BIOSENSORS INTERVENTIONAL TECHNOLOGIES PTE LTD.. The authorized representative in Taiwan is K&C 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
7727c9dacb469f3f4b564422270f03ea
Registration Details
Taiwan FDA Registration: 7727c9dacb469f3f4b564422270f03ea
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

"Belsen" Kema coronary stent system
TW: โ€œ็™พ็ˆพๆฃฎโ€ๅ…‹็‘ชๅ† ็‹€ๅ‹•่„ˆๆ”ฏๆžถ็ณป็ตฑ
Risk Class 3

Registration Details

7727c9dacb469f3f4b564422270f03ea

DHA05603304508

Company Information

Product Details

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

E Cardiovascular Medicine Science

E.0001 Cardiovascular stents

import

Dates and Status

Nov 26, 2019

Nov 26, 2029