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"StroMed" Manual Surgical Instrument for General Use (Non-Sterile) - Taiwan Registration a8e3ee3f45db2ebcaf3a6d261da578a2

Access comprehensive regulatory information for "StroMed" 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 a8e3ee3f45db2ebcaf3a6d261da578a2 and manufactured by CELL-INNOVATIONS ASIA PTY LTD. The authorized representative in Taiwan is SHINEIN BIOTECHNOLOGY CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including CELL-INNOVATIONS ASIA PTY LTD, and 1 recent registrations in the same category. 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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a8e3ee3f45db2ebcaf3a6d261da578a2
Registration Details
Taiwan FDA Registration: a8e3ee3f45db2ebcaf3a6d261da578a2
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Device Details

"StroMed" Manual Surgical Instrument for General Use (Non-Sterile)
TW: "ๆ–ฏๅพ—็พŽ" ไธ€่ˆฌๆ‰‹่ก“็”จๆ‰‹ๅ‹•ๅผๅ™จๆขฐ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

a8e3ee3f45db2ebcaf3a6d261da578a2

Ministry of Health Medical Device Import No. 020800

DHA09402080004

Company Information

Australia

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

Aug 29, 2019

Aug 29, 2024

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