"TeDan" Ear, nose, and throat fiberoptic light source and carrier (Non-Sterile) - Taiwan Registration be26bf3a385d83815ba7dd85ee0ab403
Access comprehensive regulatory information for "TeDan" Ear, nose, and throat fiberoptic light source and carrier (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 be26bf3a385d83815ba7dd85ee0ab403 and manufactured by TEDAN SURGICAL INNOVATIONS. The authorized representative in Taiwan is MYWAY INTERNATIONAL CO., LTD..
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including TEDAN SURGICAL INNOVATIONS, and 1 recent registrations in the same category. 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
be26bf3a385d83815ba7dd85ee0ab403
Ministry of Health Medical Device Import No. 016470
DHA09401647007
Product Details
G ENT device
G4350 ENT fiber optic light source and vehicle
Imported from abroad
Dates and Status
Apr 29, 2016
Apr 29, 2021
Jun 12, 2020
Cancellation Information
Logged out
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