Pure Global

"Lianfa" Auto-Lancet Lancing Device (Non-sterile) - Taiwan Registration 39a6b9bc884d88a32aed8e60d8f613e7

Access comprehensive regulatory information for "Lianfa" Auto-Lancet Lancing Device (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 39a6b9bc884d88a32aed8e60d8f613e7 and manufactured by SHANDONG LIANFA MEDICAL PLASTIC PRODUCTS CO., LTD.. The authorized representative in Taiwan is YEHSHANG ENTERPRISE CORPORATION.

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
39a6b9bc884d88a32aed8e60d8f613e7
Registration Details
Taiwan FDA Registration: 39a6b9bc884d88a32aed8e60d8f613e7
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

"Lianfa" Auto-Lancet Lancing Device (Non-sterile)
TW: "่“ฎ็™ผ"ๆŽก่ก€็ญ†(ๆœชๆป…่Œ)
Risk Class 1
MD
Cancelled

Registration Details

39a6b9bc884d88a32aed8e60d8f613e7

Ministry of Health Medical Device Land Transport No. 002117

DHA09600211707

Company Information

Product Details

I General and plastic surgical devices

I4800 General Surgery Manual Instrument

Imported from abroad; Made in China

Dates and Status

Apr 22, 2014

Apr 22, 2019

Aug 05, 2022

Cancellation Information

Logged out

ๆœชๅฑ•ๅปถ่€Œ้€พๆœŸ่€