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"Gulev" ENT fiber optic light source and vehicle (unsterilized) - Taiwan Registration fe492ff8d68fc2f6bb92e08f8a317e33

Access comprehensive regulatory information for "Gulev" ENT fiber optic light source and vehicle (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number fe492ff8d68fc2f6bb92e08f8a317e33 and manufactured by GULF MEDICAL FIBEROPTICS, INC.. The authorized representative in Taiwan is Chenyu 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.

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fe492ff8d68fc2f6bb92e08f8a317e33
Registration Details
Taiwan FDA Registration: fe492ff8d68fc2f6bb92e08f8a317e33
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Device Details

"Gulev" ENT fiber optic light source and vehicle (unsterilized)
TW: โ€œๅคๆจ‚ๅคซโ€่€ณ้ผปๅ–‰ๅ…‰็บ–ๅ…‰ๆบๅŠ่ผ‰ๅ…ท(ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

fe492ff8d68fc2f6bb92e08f8a317e33

DHA04401245501

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

Dec 07, 2012

Dec 07, 2017

Nov 20, 2019

Cancellation Information

Logged out

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