Taiwan FDA registration 9e0210207f3e15f91c1ed5084de068dd

"Sauvy" manual refractometer (unsterilized)

TW: "索維"手動折射計(未滅菌)
Taiwan flagTaiwan·Risk Class 1·TIANJIN SUOWEI ELECTRONIC TECHNOLOGY CO., LTD.·Registered Oct 01, 2021 – Oct 31, 2025Expired
Registration details
Analysis ID
9e0210207f3e15f91c1ed5084de068dd
Customs Code
DHA08600343201
Company information
Manufacturer Country
China
Product details
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
Dates and status
Registration Date
Oct 01, 2021
Expiry Date
Oct 31, 2025
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About this record

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.

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