ORIENT Corrective Spectacle Lens (Non-Sterile)
- Analysis ID
- 8bb9b374389cee83d61dd6262dd5841d
- License Form
- Ministry of Health Medical Device Import No. 017022
- Customs Code
- DHA09401702201
- Manufacturer
- FUJITA OPTICAL CO., LTD.
- Manufacturer Country
- Japan
- Authorized Representative
- Roden Optical Co., Ltd
- Product Type (Level 1)
- M Ophthalmic devices
- Product Type (Level 2)
- M5844 corrective lenses
- Import Information
- Imported from abroad
- Registration Date
- Sep 22, 2016
- Expiry Date
- Sep 22, 2026
- Cancellation Date
- Oct 20, 2022
- Status
- Logged out
- Reason
- 公司歇業
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Access comprehensive regulatory information for ORIENT 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 8bb9b374389cee83d61dd6262dd5841d and manufactured by FUJITA OPTICAL CO., LTD.. The authorized representative in Taiwan is Roden Optical Co., Ltd.
This page provides complete technical specifications, regulatory compliance details, 4 companies making similar products including OPTODEV, INC., CHEMIGLAS CORPORATION, and 5 recent registrations in the same category. 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.