"TeDan" Ear, nose, and throat fiberoptic light source and carrier (Non-Sterile)
Taiwan·Risk Class 1·MD·TEDAN SURGICAL INNOVATIONS·Registered Apr 29, 2016 – Apr 29, 2021Cancelled- Analysis ID
- be26bf3a385d83815ba7dd85ee0ab403
- License Form
- Ministry of Health Medical Device Import No. 016470
- Customs Code
- DHA09401647007
- Manufacturer
- TEDAN SURGICAL INNOVATIONS
- Manufacturer Country
- United States
- Authorized Representative
- MYWAY INTERNATIONAL CO., LTD.
- Product Type (Level 1)
- G ENT device
- Product Type (Level 2)
- G4350 ENT fiber optic light source and vehicle
- Import Information
- Imported from abroad
- Registration Date
- Apr 29, 2016
- Expiry Date
- Apr 29, 2021
- Cancellation Date
- Jun 12, 2020
- Status
- Logged out
- Reason
- 自請註銷
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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.