Pure Global

iStent Trabecular Micro-Bypass Stent System - Taiwan Registration fa92cd9fb49100a0c805e6a6743f30c5

Access comprehensive regulatory information for iStent Trabecular Micro-Bypass Stent System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number fa92cd9fb49100a0c805e6a6743f30c5 and manufactured by GLAUKOS CORPORATION. The authorized representative in Taiwan is VISION RENU 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
fa92cd9fb49100a0c805e6a6743f30c5
Registration Details
Taiwan FDA Registration: fa92cd9fb49100a0c805e6a6743f30c5
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

iStent Trabecular Micro-Bypass Stent System
TW: ๆ„›่ฆ–ๅฆๅฐๆจ‘ๅพฎๅฐŽๆตๆ”ฏๆžถ็ณป็ตฑ
Risk Class 3
MD

Registration Details

fa92cd9fb49100a0c805e6a6743f30c5

Ministry of Health Medical Device Import No. 026303

DHA05602630300

Company Information

United States

Product Details

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

M Ophthalmic devices

Imported from abroad

Dates and Status

Jul 04, 2014

Jul 04, 2024