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“Teleflex”Manual Surgical Instrument for General Use (Non-Sterile) - Taiwan Registration 3420a897cfe9d3905cea708c7e763e43

Access comprehensive regulatory information for “Teleflex”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 3420a897cfe9d3905cea708c7e763e43 and manufactured by MEDICAL SPECIALTIES, INC.. The authorized representative in Taiwan is TELEFLEX MEDICAL TAIWAN LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including KOSCHER & WÜRTZ GMBH, 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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3420a897cfe9d3905cea708c7e763e43
Registration Details
Taiwan FDA Registration: 3420a897cfe9d3905cea708c7e763e43
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Device Details

“Teleflex”Manual Surgical Instrument for General Use (Non-Sterile)
TW: “泰利福”一般手術用手動式器械 (未滅菌)
Risk Class 1
MD

Registration Details

3420a897cfe9d3905cea708c7e763e43

Ministry of Health Medical Device Import No. 021847

DHA09402184709

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

Aug 12, 2020

Aug 12, 2025

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