Pure Global

"Eccleres" laryngeal flash endoscope (unsterilized) - Taiwan Registration 4d5d58b3f49551f015c7345bc345e8ac

Access comprehensive regulatory information for "Eccleres" laryngeal flash endoscope (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 4d5d58b3f49551f015c7345bc345e8ac and manufactured by EUSA GLOBAL LLC;; ECLERIS USA. The authorized representative in Taiwan is BOYANG MEDICAL TECHNOLOGY 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
4d5d58b3f49551f015c7345bc345e8ac
Registration Details
Taiwan FDA Registration: 4d5d58b3f49551f015c7345bc345e8ac
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

"Eccleres" laryngeal flash endoscope (unsterilized)
TW: "่‰พๅ…‹่Š็†ๆ–ฏ" ๅ–‰้ ญ้–ƒ้ ปๅ…ง่ฆ–้ก (ๆœชๆป…่Œ)
Risk Class 1

Registration Details

4d5d58b3f49551f015c7345bc345e8ac

DHA09401450108

Company Information

United States

Product Details

It is limited to the first level of identification scope of the "Laryngeal Strobe Endoscopy (G.4750)" of the Measures for the Classification and Grading of Medical Devices.

G ENT Science

G.4750 Throat frequented internal mirrors

import

Dates and Status

Sep 16, 2014

Sep 16, 2029