Fore blood pen (unsterilized)
Taiwan·Risk Class 1·SHANDONG LIANFA MEDICAL PLASTIC PRODUCTS CO., LTD.·Registered Jul 29, 2019 – Jul 29, 2024Expired- Analysis ID
- c0a13cdb659018d982ed8a7558828f89
- Customs Code
- DHA09600389406
- Manufacturer Country
- China
- Authorized Representative
- TAIDOC TECHNOLOGY CORPORATION
- Intended Use
- Limited to the first level identification scope of the "Manual Instruments for General Surgery (I.4800)" of the Measures for the Classification and Grading Management of Medical Equipment.
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I.4800 Hand Instruments for General Surgery
- Import Information
- Input;; Chinese goods
- Registration Date
- Jul 29, 2019
- Expiry Date
- Jul 29, 2024
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Access comprehensive regulatory information for Fore blood pen (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number c0a13cdb659018d982ed8a7558828f89 and manufactured by SHANDONG LIANFA MEDICAL PLASTIC PRODUCTS CO., LTD.. The authorized representative in Taiwan is TAIDOC TECHNOLOGY CORPORATION.
This page provides complete technical specifications, regulatory compliance details, 2 companies making similar products including Taibo Technology Co., Ltd. five-stock factory, SHANDONG LIANFA MEDICAL PLASTIC PRODUCTS CO., LTD., 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.