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"SIDAPHARM" Manual Ophthalmic Surgical Instrument (Sterile) - Taiwan Registration 7404093426669deb1bf2467ac42eb645

Access comprehensive regulatory information for "SIDAPHARM" Manual Ophthalmic Surgical Instrument (Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 7404093426669deb1bf2467ac42eb645 and manufactured by SIDAPHARM P.C.. The authorized representative in Taiwan is EVERLIGHT INSTRUMENT 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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7404093426669deb1bf2467ac42eb645
Registration Details
Taiwan FDA Registration: 7404093426669deb1bf2467ac42eb645
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Device Details

"SIDAPHARM" Manual Ophthalmic Surgical Instrument (Sterile)
TW: "่ณฝ้”ๆ–น" ๆ‰‹ๅ‹•ๅผ็œผ็ง‘ๆ‰‹่ก“ๅ™จๆขฐ (ๆป…่Œ)
Risk Class 1
MD

Registration Details

7404093426669deb1bf2467ac42eb645

Ministry of Health Medical Device Import No. 019422

DHA09401942201

Company Information

Greece

Product Details

Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Manual Eye Surgery Instruments (M.4350)".

M Ophthalmic devices

M4350 Manual Ophthalmic Surgery Instrument

Imported from abroad

Dates and Status

Jul 27, 2018

Jul 27, 2023