"Keai Fusen" Miller Manual instruments for general surgery (unsterilized) - Taiwan Registration cd9a5b9219f47ae8c6255e22169e0fe0
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.
Device Details
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, Plastic Surgery and Dermatology
I.4800 Hand Instruments for General Surgery
import
Dates and Status
Nov 08, 2011
Nov 08, 2021
Oct 12, 2023
Cancellation Information
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