Taiwan FDA registration 8dc1e15626d37a56e6c95de8d31393fe
PENTAX Optical corrective spectacle lens (Non-Sterile)
TW: 賓德克 光學矯正鏡片 (未滅菌)
Taiwan·Risk Class 1·MD·HOYA LENS MANUFACTURING PHILIPPINES INC.·Registered Nov 02, 2016 – Nov 02, 2021CancelledRegistration details
- Analysis ID
- 8dc1e15626d37a56e6c95de8d31393fe
- License Form
- Ministry of Health Medical Device Import No. 017144
- Customs Code
- DHA09401714402
Company information
- Manufacturer
- HOYA LENS MANUFACTURING PHILIPPINES INC.
- Manufacturer Country
- Philippines
- Authorized Representative
- Wansheng Trading Co., Ltd
Product details
- Product Type (Level 1)
- M Ophthalmic devices
- Product Type (Level 2)
- M5844 corrective lenses
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Nov 02, 2016
- Expiry Date
- Nov 02, 2021
- Cancellation Date
- Sep 05, 2019
Cancellation information
- Status
- Logged out
- Reason
- 公司歇業
About this record
Access comprehensive regulatory information for PENTAX Optical corrective spectacle lens (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 8dc1e15626d37a56e6c95de8d31393fe and manufactured by HOYA LENS MANUFACTURING PHILIPPINES INC.. The authorized representative in Taiwan is Wansheng Trading Co., Ltd.
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