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"AKTIVE" Manual Ophthalmic Surgical Instrument (Non-Sterile) - Taiwan Registration c1675d236088ba4b6e0c8c7be86f9e57

Access comprehensive regulatory information for "AKTIVE" Manual Ophthalmic Surgical Instrument (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number c1675d236088ba4b6e0c8c7be86f9e57 and manufactured by AKTIVE S.R.L.. The authorized representative in Taiwan is Tiwei Wellcome Biotechnology 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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c1675d236088ba4b6e0c8c7be86f9e57
Registration Details
Taiwan FDA Registration: c1675d236088ba4b6e0c8c7be86f9e57
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Device Details

"AKTIVE" Manual Ophthalmic Surgical Instrument (Non-Sterile)
TW: "็€šๅ…‹ๆๅคซ" ๆ‰‹ๅ‹•ๅผ็œผ็ง‘ๆ‰‹่ก“ๅ™จๆขฐ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

c1675d236088ba4b6e0c8c7be86f9e57

Ministry of Health Medical Device Import No. 020012

DHA09402001205

Company Information

Italy

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

Jan 10, 2019

Jan 10, 2024