Pure Global

Pe-Ha-Luron F 3.0% - Taiwan Registration 266d3569acfa6581e42ee907238d66fa

Access comprehensive regulatory information for Pe-Ha-Luron F 3.0% in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 266d3569acfa6581e42ee907238d66fa and manufactured by Albomed GmbH. The authorized representative in Taiwan is INTELLIGENT-BIO 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
266d3569acfa6581e42ee907238d66fa
Registration Details
Taiwan FDA Registration: 266d3569acfa6581e42ee907238d66fa
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

Pe-Ha-Luron F 3.0%
TW: ๆ„›็Žป็พŽๅพทไบบๅทฅ็Žป็’ƒ้ซ”3.0%
Risk Class 3
MD

Registration Details

266d3569acfa6581e42ee907238d66fa

Ministry of Health Medical Device Import No. 029408

DHA05602940803

Company Information

Germany

Product Details

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

M Ophthalmic devices

M4275 Liquid for intraocular filling

Imported from abroad

Dates and Status

Mar 13, 2017

Mar 13, 2027