Pure Global

"Pibien" Kenle rhenium guide wire - Taiwan Registration 982ce719f2bf47a8812a0af71b218569

Access comprehensive regulatory information for "Pibien" Kenle rhenium guide wire in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 982ce719f2bf47a8812a0af71b218569 and manufactured by PBN MEDICALS DENMARK A/S. The authorized representative in Taiwan is CHINA SPRING TRADING 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
982ce719f2bf47a8812a0af71b218569
Registration Details
Taiwan FDA Registration: 982ce719f2bf47a8812a0af71b218569
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

"Pibien" Kenle rhenium guide wire
TW: "็šฎๅฟ…ๆฉ"่‚ฏๆจ‚้ŒธๅฐŽๅผ•ๅฐŽ็ทš
Risk Class 2
Cancelled

Registration Details

982ce719f2bf47a8812a0af71b218569

DHA00601154105

Company Information

Denmark

Product Details

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

E Cardiovascular Medicine Science

import

Dates and Status

Jul 12, 2005

Jul 12, 2015

Jun 25, 2018

Cancellation Information

Logged out

่จฑๅฏ่ญ‰ๅทฒ้€พๆœ‰ๆ•ˆๆœŸ