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"Taiwan Tower" Ophthalmic Scalpel (Sterilized) - Taiwan Registration f845f83dc545a2d095d53129567bb7cc

Access comprehensive regulatory information for "Taiwan Tower" Ophthalmic Scalpel (Sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number f845f83dc545a2d095d53129567bb7cc and manufactured by MANI,INC.. The authorized representative in Taiwan is TAIWAN SANTEN PHARMACEUTICAL CO., LTD..

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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f845f83dc545a2d095d53129567bb7cc
Registration Details
Taiwan FDA Registration: f845f83dc545a2d095d53129567bb7cc
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Device Details

"Taiwan Tower" Ophthalmic Scalpel (Sterilized)
TW: โ€œๅฐ็ฃๅƒๅคฉโ€ ็œผ็ง‘ๆ‰‹่ก“ๅˆ€ (ๆป…่Œ)
Risk Class 1

Registration Details

f845f83dc545a2d095d53129567bb7cc

DHA09402261608

Company Information

Japan

Product Details

Limited to the first level identification scope of the "Manual Ophthalmic Surgical Instruments (M.4350)" of the Measures for the Classification and Grading of Medical Equipment.

M Ophthalmology

M.4350 ๆ‰‹ๅ‹•ๅผ็œผ็ง‘ๆ‰‹่ก“ๅ™จๆขฐ

QMS/QSD;; ่ผธๅ…ฅ

Dates and Status

Aug 18, 2021

Aug 18, 2026