Taiwan FDA registration 2a610a06512a9e202d5d8d709cb3859a
"SEIKO" corrective spectacle lens (Non-sterile)
TW: "精功" 矯正鏡片 (未滅菌)
Taiwan·Risk Class 1·MD·SEIKO HOLDINGS CORPORATION·Registered Nov 15, 2016 – Nov 15, 2021ExpiredRegistration details
- Analysis ID
- 2a610a06512a9e202d5d8d709cb3859a
- License Form
- Ministry of Health Medical Device Import No. 017175
- Customs Code
- DHA09401717500
Company information
- Manufacturer
- SEIKO HOLDINGS CORPORATION
- Manufacturer Country
- Japan
- Authorized Representative
- Tokyo Optical Co., Ltd. Taipei store
Product details
- Intended Use
- Limited to the first level identification range of the Measures for the Administration of Medical Devices "Corrective Lenses (M.5844)".
- 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 15, 2016
- Expiry Date
- Nov 15, 2021
About this record
Access comprehensive regulatory information for "SEIKO" 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 2a610a06512a9e202d5d8d709cb3859a and manufactured by SEIKO HOLDINGS CORPORATION. The authorized representative in Taiwan is Tokyo Optical Co., Ltd. Taipei store.
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