Taiwan FDA registration 2fef3ba64a19e4a540f2b3395a430eff
"San Nishimura" Trial Lens Set (Non-Sterile)
TW: "桑尼西姆納" 試鏡組 (未滅菌)
Registration details
- Analysis ID
- 2fef3ba64a19e4a540f2b3395a430eff
- License Form
- Ministry of Health Medical Device Import No. 016787
- Customs Code
- DHA09401678700
Company information
- Manufacturer
- SAN NISHIMURA CO., LTD.
- Manufacturer Country
- Japan
- Authorized Representative
- IKI MEDICAL CO., LTD.
Product details
- Intended Use
- Limited to the first level recognition range of the ophthalmic test lens group (M.1405) of the Measures for the Administration of Medical Devices.
- Product Type (Level 1)
- M Ophthalmic devices
- Product Type (Level 2)
- M1405 Ophthalmic Test Lens Group
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jul 15, 2016
- Expiry Date
- Jul 15, 2021
About this record
Access comprehensive regulatory information for "San Nishimura" Trial Lens Set (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 2fef3ba64a19e4a540f2b3395a430eff and manufactured by SAN NISHIMURA CO., LTD.. The authorized representative in Taiwan is IKI MEDICAL CO., LTD..
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