"Telifes" manual instruments for general surgery (unsterilized)
Taiwan·Risk Class 1·TELEFLEX MEDICAL·Registered Sep 19, 2008 – Sep 19, 2023Expired- Analysis ID
- 4bb8fbda26f9a0891ca75afe47034848
- Customs Code
- DHA04400708102
- Manufacturer
- TELEFLEX MEDICAL
- Manufacturer Country
- United States
- Authorized Representative
- Huizhong 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, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I.4800 Hand Instruments for General Surgery
- Import Information
- import
- Registration Date
- Sep 19, 2008
- Expiry Date
- Sep 19, 2023
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Access comprehensive regulatory information for "Telifes" 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 4bb8fbda26f9a0891ca75afe47034848 and manufactured by TELEFLEX MEDICAL. The authorized representative in Taiwan is Huizhong Co., Ltd.
This page provides complete technical specifications, regulatory compliance details, 2 companies making similar products including Teleflex Medical, HUDSON RESPIRATORY CARE TECATE S. DE R.L. DE C.V.(A TELEFLEX MEDICAL COMPANY), 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.