Wuding blood collection device (unsterilized)
Taiwan·Risk Class 1·OWEN MUMFORD LIMITED·Registered Jul 13, 2022 – Jul 13, 2027Active- Analysis ID
- f32730bf9907ad4f6f2eb007d4ceeaa3
- Customs Code
- DHA09402285207
- Manufacturer
- OWEN MUMFORD LIMITED
- Manufacturer Country
- United Kingdom
- Authorized Representative
- APEX BIOTECHNOLOGY 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
- QMS/QSD;; 輸入
- Registration Date
- Jul 13, 2022
- Expiry Date
- Jul 13, 2027
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Access comprehensive regulatory information for Wuding blood collection device (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number f32730bf9907ad4f6f2eb007d4ceeaa3 and manufactured by OWEN MUMFORD LIMITED. The authorized representative in Taiwan is APEX BIOTECHNOLOGY CORPORATION.
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including GMMC, 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.