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Yeson Technology Surgical glasses (magnifying glass) (unsterilized) - Taiwan Registration 03804b744324531ba1c8de7622366632

Access comprehensive regulatory information for Yeson Technology Surgical glasses (magnifying glass) (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 03804b744324531ba1c8de7622366632 and manufactured by QUALITY ASPIRATORS, INC.. The authorized representative in Taiwan is CORNUCOPIA INNOVATION CORPORATION.

This page provides complete technical specifications, regulatory compliance details. 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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03804b744324531ba1c8de7622366632
Registration Details
Taiwan FDA Registration: 03804b744324531ba1c8de7622366632
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Device Details

Yeson Technology Surgical glasses (magnifying glass) (unsterilized)
TW: ๆฅญ็”Ÿ็ง‘ๆŠ€ ๆ‰‹่ก“็œผ้ก(ๆ”พๅคง้ก) (ๆœชๆป…่Œ)
Risk Class 1

Registration Details

03804b744324531ba1c8de7622366632

DHA084a0008709

Company Information

United States

Product Details

Limited to the first level of classification and grading management of medical devices, "Ophthalmic surgical glasses (magnifying glasses) (M.4770)".

M Ophthalmology

M.4770 Ophthalmic surgical lenses (magnifying lenses)

Dates and Status

Feb 12, 2022

Oct 31, 2025