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"Day Fiber" ENT fiber optic light source system - Taiwan Registration 153c57d3ef60c8819a80f9dfb48835fd

Access comprehensive regulatory information for "Day Fiber" ENT fiber optic light source system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 153c57d3ef60c8819a80f9dfb48835fd and manufactured by SUNOPTIC TECHNOLOGIES. The authorized representative in Taiwan is PRO-READY ENTERPRISE 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.

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153c57d3ef60c8819a80f9dfb48835fd
Registration Details
Taiwan FDA Registration: 153c57d3ef60c8819a80f9dfb48835fd
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Device Details

"Day Fiber" ENT fiber optic light source system
TW: "ๆ—ฅๅ…‰็บ–" ่€ณ้ผปๅ–‰ๅ…‰็บ–ๅ…‰ๆบ็ณป็ตฑ
Risk Class 1
Cancelled

Registration Details

153c57d3ef60c8819a80f9dfb48835fd

DHA04400356504

Company Information

United States

Product Details

Limited to the first level identification scope of the Measures for the Administration of Medical Devices "ENT Fiber Optic Light Source and Vehicle (G.4350)".

G ENT Science

G.4350 Ear, nose and throat optical fiber light sources and carriers

import

Dates and Status

Apr 11, 2006

Apr 11, 2011

Oct 31, 2012

Cancellation Information

Logged out

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