Pure Global

"Delden" root tube paper needle (unsterilized) - Taiwan Registration 0b9f33caed75674a5076b4cbe204e9bc

Access comprehensive regulatory information for "Delden" root tube paper needle (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 0b9f33caed75674a5076b4cbe204e9bc and manufactured by DIADENT GROUP INTERNATIONAL. The authorized representative in Taiwan is MODFIT ENTERPRISE 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
0b9f33caed75674a5076b4cbe204e9bc
Registration Details
Taiwan FDA Registration: 0b9f33caed75674a5076b4cbe204e9bc
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

"Delden" root tube paper needle (unsterilized)
TW: โ€œๅฒฑ็ˆพ็™ปโ€ๆ น็ฎก็ด™้‡(ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

0b9f33caed75674a5076b4cbe204e9bc

DHA04401046902

Company Information

Korea, Republic of

Product Details

Limited to the first level identification range of the Measures for the Administration of Medical Devices "Root Canal Paper Needle (F.3830)".

F Dentistry

F.3830 Root Canal

import

Dates and Status

Jun 13, 2011

Jun 13, 2016

May 17, 2018

Cancellation Information

Logged out

่จฑๅฏ่ญ‰ๅทฒ้€พๆœ‰ๆ•ˆๆœŸ