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“CareFusion” V. Mueller Manual surgical instrument for general use (Non-Sterile) - Taiwan Registration d7ed57f57de5bcacb5a337697d0879c7

Access comprehensive regulatory information for “CareFusion” V. Mueller 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 d7ed57f57de5bcacb5a337697d0879c7 and manufactured by CareFusion Germany 318 GmbH. The authorized representative in Taiwan is BESPRING INTERNATIONAL MARKETING CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 2 companies making similar products including CAREFUSION, CareFusion, and 2 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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d7ed57f57de5bcacb5a337697d0879c7
Registration Details
Taiwan FDA Registration: d7ed57f57de5bcacb5a337697d0879c7
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Device Details

“CareFusion” V. Mueller Manual surgical instrument for general use (Non-Sterile)
TW: “客愛福生”密米樂一般手術用手動式器械(未滅菌)
Risk Class 1
MD

Registration Details

d7ed57f57de5bcacb5a337697d0879c7

Ministry of Health Medical Device Import No. 020183

DHA09402018306

Company Information

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

Mar 14, 2019

Mar 14, 2024

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