Taiwan FDA registration 1d5ece7617df5509e0e3f08edfca5c56
"BenQ Mitoyo" respirator tubing (unsterilized)
TW: "明基三豐" 呼吸器管路 (未滅菌)
Taiwan·Risk Class 1·HSINER CO., LTD.·Registered Jul 24, 2012 – Jul 24, 2027ActiveRegistration details
- Analysis ID
- 1d5ece7617df5509e0e3f08edfca5c56
Company information
- Manufacturer
- HSINER CO., LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- BENQ MEDICAL TECHNOLOGY CORPORATION
Product details
- Intended Use
- Limited to the first level identification range of the "Respirator Pipeline (D.5975)" of the Measures for the Classification and Grading Management of Medical Equipment.
- Product Type (Level 1)
- D Anesthesiology
- Product Type (Level 2)
- D.5975 Respirator Tubing
- Import Information
- QMS/QSD;; 委託製造;; 國產
Dates and status
- Registration Date
- Jul 24, 2012
- Expiry Date
- Jul 24, 2027
About this record
Access comprehensive regulatory information for "BenQ Mitoyo" respirator tubing (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 1d5ece7617df5509e0e3f08edfca5c56 and manufactured by HSINER CO., LTD.. The authorized representative in Taiwan is BENQ MEDICAL TECHNOLOGY CORPORATION.
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