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"Hanktif" Manual Eye Surgery Instruments (Sterile/Unsterile) - Taiwan Registration ca6846d853b0b969c0e99807255e3221

Access comprehensive regulatory information for "Hanktif" Manual Eye Surgery Instruments (Sterile/Unsterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number ca6846d853b0b969c0e99807255e3221 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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ca6846d853b0b969c0e99807255e3221
Registration Details
Taiwan FDA Registration: ca6846d853b0b969c0e99807255e3221
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Device Details

"Hanktif" Manual Eye Surgery Instruments (Sterile/Unsterile)
TW: "็€šๅ…‹ๆๅคซ" ๆ‰‹ๅ‹•ๅผ็œผ็ง‘ๆ‰‹่ก“ๅ™จๆขฐ (ๆป…่Œ/ๆœชๆป…่Œ)
Risk Class 1

Registration Details

ca6846d853b0b969c0e99807255e3221

DHA09402101006

Company Information

Italy

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

Input;; QMS/QSD

Dates and Status

Nov 07, 2019

Nov 07, 2024