Taiwan FDA registration 80013cfae8781615e9755b7bdb6d2345
"DVI" Ear, nose, and throat fiberoptic light source and carrier (Non-Sterile)
TW: "第維愛" 耳鼻喉光纖光源及載具 (未滅菌)
Taiwan·Risk Class 1·MD·DESIGNS FOR VISION, INC.·Registered Jul 28, 2016 – Jul 28, 2021ExpiredRegistration details
- Analysis ID
- 80013cfae8781615e9755b7bdb6d2345
- License Form
- Ministry of Health Medical Device Import No. 016834
- Customs Code
- DHA09401683406
Company information
- Manufacturer
- DESIGNS FOR VISION, INC.
- Manufacturer Country
- United States
- Authorized Representative
- Liren Equipment Factory Co., Ltd
Product details
- Intended Use
- Limited to the first level identification scope of the Measures for the Administration of Medical Devices "ENT Fiber Optic Light Source and Vehicle (G.4350)".
- Product Type (Level 1)
- G ENT device
- Product Type (Level 2)
- G4350 ENT fiber optic light source and vehicle
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jul 28, 2016
- Expiry Date
- Jul 28, 2021
About this record
Access comprehensive regulatory information for "DVI" 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 80013cfae8781615e9755b7bdb6d2345 and manufactured by DESIGNS FOR VISION, INC.. The authorized representative in Taiwan is Liren Equipment Factory Co., Ltd.
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