"Gyrus" Ear, nose, and throat examination and treatment unit (Non-Sterile) - Taiwan Registration da21ec150e53d8da417eaa5ba4696f4c
Access comprehensive regulatory information for "Gyrus" Ear, nose, and throat examination and treatment unit (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number da21ec150e53d8da417eaa5ba4696f4c and manufactured by GYRUS MEDICAL GMBH. The authorized representative in Taiwan is Yuanyou Industrial 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.
Device Details
Registration Details
da21ec150e53d8da417eaa5ba4696f4c
Ministry of Health Medical Device Import No. 013391
DHA09401339109
Product Details
G ENT device
G5300 ENT Examination and Treatment Unit
Imported from abroad
Dates and Status
Sep 06, 2013
Sep 06, 2018
Aug 05, 2022
Cancellation Information
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