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"Cuisley" fiber optic light source and vehicle (unsterilized) - Taiwan Registration 2cb8c1ce7b5ed0d9c7186783ed1e9621

Access comprehensive regulatory information for "Cuisley" 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 2cb8c1ce7b5ed0d9c7186783ed1e9621 and manufactured by TRANSLITE. The authorized representative in Taiwan is GETZ BROS & CO. (BVI), INC., TAIWAN BRANCH.

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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2cb8c1ce7b5ed0d9c7186783ed1e9621
Registration Details
Taiwan FDA Registration: 2cb8c1ce7b5ed0d9c7186783ed1e9621
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Device Details

"Cuisley" fiber optic light source and vehicle (unsterilized)
TW: โ€œ่ƒๆ–ฏ้›ทโ€ๅ…‰็บ–ๅ…‰ๆบๅŠ่ผ‰ๅ…ท(ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

2cb8c1ce7b5ed0d9c7186783ed1e9621

DHA04400641003

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 21, 2007

Dec 21, 2012

Apr 15, 2014

Cancellation Information

Logged out

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