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“Teleflex”Manual Surgical Instrument for General Use (Non-Sterile) - Taiwan Registration 6a6fe8ca553e051d369c713f4775cec6

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 6a6fe8ca553e051d369c713f4775cec6 and manufactured by KOSCHER & WÜRTZ GMBH. 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 MEDICAL SPECIALTIES, INC., 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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6a6fe8ca553e051d369c713f4775cec6
Registration Details
Taiwan FDA Registration: 6a6fe8ca553e051d369c713f4775cec6
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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

6a6fe8ca553e051d369c713f4775cec6

Ministry of Health Medical Device Import No. 018818

DHA09401881805

Company Information

Germany

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

Feb 13, 2018

Feb 13, 2028

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