"Keai Fusen" Miller Manual instruments for general surgery (unsterilized)
Taiwan·Risk Class 1·CAREFUSION GERMANY 318 GMBH·Registered Nov 08, 2011 – Nov 08, 2021Cancelled- Analysis ID
- cd9a5b9219f47ae8c6255e22169e0fe0
- Customs Code
- DHA04401103000
- Manufacturer
- CAREFUSION GERMANY 318 GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- CHAMPION MEDICAL CORPORATION
- 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, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I.4800 Hand Instruments for General Surgery
- Import Information
- import
- Registration Date
- Nov 08, 2011
- Expiry Date
- Nov 08, 2021
- Cancellation Date
- Oct 12, 2023
- Status
- Logged out
- Reason
- 未展延而逾期者
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Access comprehensive regulatory information for "Keai Fusen" Miller Manual instruments for general surgery (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number cd9a5b9219f47ae8c6255e22169e0fe0 and manufactured by CAREFUSION GERMANY 318 GMBH. The authorized representative in Taiwan is CHAMPION MEDICAL CORPORATION.
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including CAREFUSION, 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.