Pure Global

"Atrium" Vascular Tunneler (Non-Sterile) - Taiwan Registration 5f82adf962066e7d2ed24fa6421dba1a

Access comprehensive regulatory information for "Atrium" Vascular Tunneler (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 5f82adf962066e7d2ed24fa6421dba1a and manufactured by Atrium Medical Corporation. The authorized representative in Taiwan is GETINGE GROUP TAIWAN 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
5f82adf962066e7d2ed24fa6421dba1a
Registration Details
Taiwan FDA Registration: 5f82adf962066e7d2ed24fa6421dba1a
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

"Atrium" Vascular Tunneler (Non-Sterile)
TW: "ไบž็ฟ ๆฉ"่ก€็ฎก้šง้“ๅ™จ(ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

5f82adf962066e7d2ed24fa6421dba1a

Ministry of Health Medical Device Import No. 018600

DHA09401860004

Company Information

United States

Product Details

Limited to the first level identification range of medical equipment management measures for cardiovascular surgical instruments (E.4500).

E Cardiovascular devices

E4500 Cardiovascular Surgical Instrument

Imported from abroad

Dates and Status

Dec 12, 2017

Dec 12, 2027