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"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.

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be26bf3a385d83815ba7dd85ee0ab403
Registration Details
Taiwan FDA Registration: be26bf3a385d83815ba7dd85ee0ab403
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Device Details

"TeDan" Ear, nose, and throat fiberoptic light source and carrier (Non-Sterile)
TW: "็ทนๅธๅฎ‰" ่€ณ้ผปๅ–‰ๅ…‰็บ–ๅ…‰ๆบๅŠ่ผ‰ๅ…ท (ๆœชๆป…่Œ)
Risk Class 1
MD
Cancelled

Registration Details

be26bf3a385d83815ba7dd85ee0ab403

Ministry of Health Medical Device Import No. 016470

DHA09401647007

Company Information

United States

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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