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"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.

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da21ec150e53d8da417eaa5ba4696f4c
Registration Details
Taiwan FDA Registration: da21ec150e53d8da417eaa5ba4696f4c
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Device Details

"Gyrus" Ear, nose, and throat examination and treatment unit (Non-Sterile)
TW: "ๅ‰ๆด›ๆฐ" ่€ณ้ผปๅ–‰ๆชขๆŸฅๅŠๆฒป็™‚ๆชฏ (ๆœชๆป…่Œ)
Risk Class 1
MD
Cancelled

Registration Details

da21ec150e53d8da417eaa5ba4696f4c

Ministry of Health Medical Device Import No. 013391

DHA09401339109

Company Information

Germany

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

Logged out

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