Taiwan FDA registration a8e3ee3f45db2ebcaf3a6d261da578a2

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

TW: "斯得美" 一般手術用手動式器械 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·CELL-INNOVATIONS ASIA PTY LTD·Registered Aug 29, 2019 – Aug 29, 2024Expired
Registration details
Analysis ID
a8e3ee3f45db2ebcaf3a6d261da578a2
License Form
Ministry of Health Medical Device Import No. 020800
Customs Code
DHA09402080004
Company information
Manufacturer Country
Australia
Authorized Representative
SHINEIN BIOTECHNOLOGY CO., LTD.
Product details
Intended Use
Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Manual Instruments for General Surgery (I.4800)".
Product Type (Level 1)
I General and plastic surgical devices
Product Type (Level 2)
I4800 General Surgery Manual Instrument
Import Information
Imported from abroad
Dates and status
Registration Date
Aug 29, 2019
Expiry Date
Aug 29, 2024
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About this record

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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