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"HEIWA" Manual surgical instrument for general use (Non-Sterile) - Taiwan Registration b291b273c4e77d93daa4ea346265da40

Access comprehensive regulatory information for "HEIWA" 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 b291b273c4e77d93daa4ea346265da40 and manufactured by HEIWA MEDICAL INSTRUMENTS CO., LTD.. The authorized representative in Taiwan is HEALTH RIVER INC..

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b291b273c4e77d93daa4ea346265da40
Registration Details
Taiwan FDA Registration: b291b273c4e77d93daa4ea346265da40
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Device Details

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

Registration Details

b291b273c4e77d93daa4ea346265da40

Ministry of Health Medical Device Import No. 017908

DHA09401790801

Company Information

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

Jun 02, 2017

Jun 02, 2027