"Sauvy" manual refractometer (unsterilized)
- Analysis ID
- 9e0210207f3e15f91c1ed5084de068dd
- Customs Code
- DHA08600343201
- Manufacturer
- TIANJIN SUOWEI ELECTRONIC TECHNOLOGY CO., LTD.
- Manufacturer Country
- China
- Authorized Representative
- Kang Cheng Medical Technology Co., Ltd
- Intended Use
- It is limited to the first-level identification scope of the "Manual Refractor (M.1770)" of the Administrative Measures for the Classification and Grading of Medical Devices.
- Product Type (Level 1)
- M Ophthalmology
- Product Type (Level 2)
- M.1770 手動式驗光儀
- Import Information
- Input;; Chinese goods;; QMS/QSD
- Registration Date
- Oct 01, 2021
- Expiry Date
- Oct 31, 2025
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Access comprehensive regulatory information for "Sauvy" manual refractometer (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 9e0210207f3e15f91c1ed5084de068dd and manufactured by TIANJIN SUOWEI ELECTRONIC TECHNOLOGY CO., LTD.. The authorized representative in Taiwan is Kang Cheng Medical Technology Co., Ltd.
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including TIANJIN SUOWEI ELECTRONIC TECHNOLOGY CO., LTD., and 1 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.