Pure Global

"HDI" GingiCord Retraction cord (Non-Sterile) - Taiwan Registration 3f7130b22a484eb6785d0b52a291d0d6

Access comprehensive regulatory information for "HDI" GingiCord Retraction cord (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 3f7130b22a484eb6785d0b52a291d0d6 and manufactured by HDI INC.. The authorized representative in Taiwan is MNM BIOTECHNOLOGY 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
3f7130b22a484eb6785d0b52a291d0d6
Registration Details
Taiwan FDA Registration: 3f7130b22a484eb6785d0b52a291d0d6
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

"HDI" GingiCord Retraction cord (Non-Sterile)
TW: "่‰พๅ–ๅพท" ้‡‘ๅ‰ๅฏๆŽ’้ฝฆ็ทš(ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

3f7130b22a484eb6785d0b52a291d0d6

Ministry of Health Medical Device Import No. 018761

DHA09401876102

Company Information

Korea, Republic of

Product Details

Limited to the first level identification range of the gingival line (F.0001) of the medical equipment management method.

F Dental devices

F0001 Gingival drain line

Imported from abroad

Dates and Status

Jan 25, 2018

Jan 25, 2028