"TeDan" Ear, nose, and throat fiberoptic light source and carrier (Non-Sterile)
Taiwan·Risk Class 1·MD·TEDAN SURGICAL INNOVATIONS·Registered Aug 11, 2014 – Aug 11, 2019Cancelled- Analysis ID
- 94b6afd1b24f2a2e8911d8915f7a9abb
- License Form
- Ministry of Health Medical Device Import No. 014427
- Customs Code
- DHA09401442709
- Manufacturer
- TEDAN SURGICAL INNOVATIONS
- Manufacturer Country
- United States
- Authorized Representative
- Ryan Medical Devices 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
- Aug 11, 2014
- Expiry Date
- Aug 11, 2019
- Cancellation Date
- Jul 15, 2022
- Status
- Logged out
- Reason
- 未展延而逾期者
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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 94b6afd1b24f2a2e8911d8915f7a9abb and manufactured by TEDAN SURGICAL INNOVATIONS. The authorized representative in Taiwan is Ryan Medical Devices 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.