“CareFusion” V. Mueller Manual surgical instrument for general use (Non-Sterile)
Taiwan·Risk Class 1·MD·CareFusion Germany 318 GmbH·Registered Mar 14, 2019 – Mar 14, 2024Expired- Analysis ID
- d7ed57f57de5bcacb5a337697d0879c7
- License Form
- Ministry of Health Medical Device Import No. 020183
- Customs Code
- DHA09402018306
- Manufacturer
- CareFusion Germany 318 GmbH
- Manufacturer Country
- Germany
- Authorized Representative
- BESPRING INTERNATIONAL MARKETING CO., LTD.
- 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
- Registration Date
- Mar 14, 2019
- Expiry Date
- Mar 14, 2024
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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.