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"Buffalo Filter"Manual Surgical Instrument for General Use (Non-Sterile) - Taiwan Registration 89e9673cd824fe54ecb9a4b9979b43e4

Access comprehensive regulatory information for "Buffalo Filter"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 89e9673cd824fe54ecb9a4b9979b43e4 and manufactured by BUFFALO FILTER LLC. The authorized representative in Taiwan is Huizhong 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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89e9673cd824fe54ecb9a4b9979b43e4
Registration Details
Taiwan FDA Registration: 89e9673cd824fe54ecb9a4b9979b43e4
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Device Details

"Buffalo Filter"Manual Surgical Instrument for General Use (Non-Sterile)
TW: "ๅทด่Š™ๆด›"ไธ€่ˆฌๆ‰‹่ก“็”จๆ‰‹ๅ‹•ๅผๅ™จๆขฐ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

89e9673cd824fe54ecb9a4b9979b43e4

Ministry of Health Medical Device Import No. 019973

DHA09401997309

Company Information

United States

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

Dec 27, 2018

Dec 27, 2023