Taiwan FDA registration 5ea5bf1d60a6e45670f2b1805f8befae
Revision Overnight Wear Orthokeratology Contact Lens
TW: 銳視夜戴型角膜塑型隱形眼鏡
Taiwan·Risk Class 3·MD·Eagle Vision Co., Ltd. Shilin Factory·Registered May 14, 2020 – Dec 19, 2027ActiveRegistration details
- Analysis ID
- 5ea5bf1d60a6e45670f2b1805f8befae
- License Form
- Ministry of Health Medical Device Manufacturing No. 006792
Company information
- Manufacturer
- Eagle Vision Co., Ltd. Shilin Factory
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- VISION TECHNOLOGY CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- M Ophthalmic devices
- Product Type (Level 2)
- M5916 Rigid breathable contact lens
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- May 14, 2020
- Expiry Date
- Dec 19, 2027
About this record
Access comprehensive regulatory information for Revision Overnight Wear Orthokeratology Contact Lens in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 5ea5bf1d60a6e45670f2b1805f8befae and manufactured by Eagle Vision Co., Ltd. Shilin Factory. The authorized representative in Taiwan is VISION TECHNOLOGY CO., LTD..
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