Pure Global

“NeuLight” Holmium Laser Fibers - Taiwan Registration 58406e5a38b1b56b8ae22d7cfcc01e3b

Access comprehensive regulatory information for “NeuLight” Holmium Laser Fibers in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 58406e5a38b1b56b8ae22d7cfcc01e3b and manufactured by WEINERT Fiber Optics, Inc.. The authorized representative in Taiwan is JIANHE BIO-MEDICAL 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
58406e5a38b1b56b8ae22d7cfcc01e3b
Registration Details
Taiwan FDA Registration: 58406e5a38b1b56b8ae22d7cfcc01e3b
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

“NeuLight” Holmium Laser Fibers
TW: “紐萊特”雷射光纖
Risk Class 2
MD

Registration Details

58406e5a38b1b56b8ae22d7cfcc01e3b

Ministry of Health Medical Device Import No. 036805

DHA05603680504

Company Information

United States

Product Details

Details are as detailed as approved Chinese instructions

I General, Plastic Surgery and Dermatology

I4810 Lasers for general surgery, plastic surgery and dermatology

Imported from abroad

Dates and Status

Oct 13, 2023

Oct 13, 2028