Taiwan FDA registration 1e7d774e0032a5d73796c0a3e9ad1493
"Surgical propulsion" propulsion (sterile)
TW: “術捷” 義乳推進器 (滅菌)
Taiwan·Risk Class 1·SHINEO TECHNOLOGY CO., LTD.·Registered Oct 28, 2020 – Oct 28, 2025ExpiredRegistration details
- Analysis ID
- 1e7d774e0032a5d73796c0a3e9ad1493
Company information
- Manufacturer
- SHINEO TECHNOLOGY CO., LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- BIOTEGY CORPORATION
Product details
- 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
- 國產;; 委託製造;; QMS/QSD
Dates and status
- Registration Date
- Oct 28, 2020
- Expiry Date
- Oct 28, 2025
About this record
Access comprehensive regulatory information for "Surgical propulsion" propulsion (sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 1e7d774e0032a5d73796c0a3e9ad1493 and manufactured by SHINEO TECHNOLOGY CO., LTD.. The authorized representative in Taiwan is BIOTEGY CORPORATION.
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