Taiwan FDA registration c0cdd462075991bbff871825c4f384b0
PENTAX corrective spectacle lens (Non-Sterile)
TW: 賓德克 矯正鏡片 (未滅菌)
Taiwan·Risk Class 1·MD·HOYA LENS MANUFACTURING PHILIPPINES INC.·Registered Jun 16, 2014 – Jun 16, 2019CancelledRegistration details
- Analysis ID
- c0cdd462075991bbff871825c4f384b0
- License Form
- Ministry of Health Medical Device Import No. 014255
- Customs Code
- DHA09401425506
Company information
- Manufacturer
- HOYA LENS MANUFACTURING PHILIPPINES INC.
- Manufacturer Country
- Philippines
- Authorized Representative
- HOYA LENS TAIWAN 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
- Jun 16, 2014
- Expiry Date
- Jun 16, 2019
- Cancellation Date
- Jun 22, 2022
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for PENTAX 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 c0cdd462075991bbff871825c4f384b0 and manufactured by HOYA LENS MANUFACTURING PHILIPPINES INC.. The authorized representative in Taiwan is HOYA LENS TAIWAN LTD..
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