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"Hankil" Manual surgical instrument for general use (Non-Sterile) - Taiwan Registration 90240d5dd785c3e99131f32ddaefaf30

Access comprehensive regulatory information for "Hankil" Manual surgical instrument for general use (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 90240d5dd785c3e99131f32ddaefaf30 and manufactured by HANKIL TECH MEDICAL CO., LTD.. The authorized representative in Taiwan is DE LI BIOTECHNOLOGY CO., LTD..

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90240d5dd785c3e99131f32ddaefaf30
Registration Details
Taiwan FDA Registration: 90240d5dd785c3e99131f32ddaefaf30
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Device Details

"Hankil" Manual surgical instrument for general use (Non-Sterile)
TW: "ๆผขๅฅ‡" ไธ€่ˆฌๆ‰‹่ก“็”จๆ‰‹ๅ‹•ๅผๅ™จๆขฐ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

90240d5dd785c3e99131f32ddaefaf30

Ministry of Health Medical Device Import No. 016831

DHA09401683100

Company Information

Korea, Republic of

Product Details

Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Manual Instruments for General Surgery (I.4800)".

I General and plastic surgical devices

I4800 General Surgery Manual Instrument

Imported from abroad

Dates and Status

Jul 27, 2016

Jul 27, 2026