“Teleflex”Manual Surgical Instrument for General Use (Non-Sterile)
Taiwan·Risk Class 1·MD·KOSCHER & WÜRTZ GMBH·Registered Feb 13, 2018 – Feb 13, 2028Active- Analysis ID
- 6a6fe8ca553e051d369c713f4775cec6
- License Form
- Ministry of Health Medical Device Import No. 018818
- Customs Code
- DHA09401881805
- Manufacturer
- KOSCHER & WÜRTZ GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- TELEFLEX MEDICAL TAIWAN 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
- Feb 13, 2018
- Expiry Date
- Feb 13, 2028
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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.