Taiwan FDA registration 919da9d2f97d5b4618a1e04256740492
BUTICON UV Daily Disposable Contact Lens(All Day)
TW: 美麗康每日拋棄式隱形眼鏡
Taiwan·Risk Class 2·MD·Park Branch of Canamé Optics Co., Ltd·Registered Aug 11, 2017 – Oct 14, 2020CancelledRegistration details
- Analysis ID
- 919da9d2f97d5b4618a1e04256740492
- License Form
- Ministry of Health Medical Device Manufacturing No. 005846
Company information
- Manufacturer
- Park Branch of Canamé Optics Co., Ltd
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- CAMAX OPTICAL CORP.
Product details
- Product Type (Level 1)
- M Ophthalmic devices
- Product Type (Level 2)
- M5925 Flexible Contact Lens
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- Aug 11, 2017
- Expiry Date
- Oct 14, 2020
- Cancellation Date
- Mar 29, 2021
Cancellation information
- Status
- Logged out
- Reason
- 自請註銷
About this record
Access comprehensive regulatory information for BUTICON UV Daily Disposable Contact Lens(All Day) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 919da9d2f97d5b4618a1e04256740492 and manufactured by Park Branch of Canamé Optics Co., Ltd. The authorized representative in Taiwan is CAMAX OPTICAL CORP..
This page provides complete technical specifications, regulatory compliance details. 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.
Free DatabasePowered by Pure Global AI89,000+ Devices