Taiwan FDA registration ba01b54990415c31a523749e9deb8884

"Adetica" manual refractometer (unsterilized)

TW: "阿德緹卡" 手動折射計 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·Adaptica S. r. l.·Registered Oct 04, 2019 – Oct 04, 2024Cancelled
Registration details
Analysis ID
ba01b54990415c31a523749e9deb8884
Customs Code
DHA09402092501
Company information
Manufacturer
Adaptica S. r. l.
Manufacturer Country
Italy
Authorized Representative
EVERLIGHT INSTRUMENT CO., LTD.
Product details
Intended Use
Limited to the first level identification range of the Measures for the Administration of Medical Devices "Manual Refractometer (M.1770)".
Product Type (Level 1)
M Ophthalmology
Product Type (Level 2)
M.1770 手動式驗光儀
Import Information
Input;; QMS/QSD
Dates and status
Registration Date
Oct 04, 2019
Expiry Date
Oct 04, 2024
Cancellation Date
Sep 30, 2021
Cancellation information
Status
Logged out
Reason
轉為登錄字號
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About this record

Access comprehensive regulatory information for "Adetica" 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 ba01b54990415c31a523749e9deb8884 and manufactured by Adaptica S. r. l.. The authorized representative in Taiwan is EVERLIGHT INSTRUMENT CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including Adaptica S. r. l., 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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