"Sevis corrective lenses" (unsterilized)
- Analysis ID
- 5b9f188b06d850c0b2b640fa01e80e44
- Customs Code
- DHA04600122104
- Manufacturer Country
- China
- Authorized Representative
- Handong Technology Co., Ltd
- 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 Ophthalmology
- Product Type (Level 2)
- M.5844 corrective lenses
- Import Information
- Chinese goods;; Input;; Contract manufacturing
- Registration Date
- Dec 27, 2010
- Expiry Date
- Dec 27, 2015
- Cancellation Date
- Aug 09, 2018
- Status
- Logged out
- Reason
- 未展延而逾期者
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Access comprehensive regulatory information for "Sevis corrective lenses" (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 5b9f188b06d850c0b2b640fa01e80e44 and manufactured by DANYANG TIANMU OPTICAL GLASSES CO., LTD.;; XINXIANG SINWEI TRADING CO., LTD.. The authorized representative in Taiwan is Handong Technology Co., Ltd.
This page provides complete technical specifications, regulatory compliance details, 2 companies making similar products including HANMI SWISS OPTICAL GLASSES CO., LTD, Singapore Merchant Mind Optical Co., Ltd. Taiwan Branch, and 2 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.