Pure Global

"Graceful" bulbous vasodilated duct - Taiwan Registration ba89dc51ed7e14450aa1b2c45d38e236

Access comprehensive regulatory information for "Graceful" bulbous vasodilated duct in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number ba89dc51ed7e14450aa1b2c45d38e236 and manufactured by NUMED INC.. The authorized representative in Taiwan is SILVER BELL ENTERPRISE INC..

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
ba89dc51ed7e14450aa1b2c45d38e236
Registration Details
Taiwan FDA Registration: ba89dc51ed7e14450aa1b2c45d38e236
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

"Graceful" bulbous vasodilated duct
TW: โ€œๅ„ช็พŽโ€็ƒไธญ็ƒ่ก€็ฎกๆ“ดๅผตๅฐŽ็ฎก
Risk Class 2
Cancelled

Registration Details

ba89dc51ed7e14450aa1b2c45d38e236

DHA00601989400

Company Information

United States

Product Details

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

E Cardiovascular Medicine Science

E.1250 Percutaneous catheters

import

Dates and Status

Jun 08, 2009

Jun 08, 2019

May 19, 2022

Cancellation Information

Logged out

่‡ช่กŒ้ตๅ…ฅ