Taiwan FDA registration c92b721ba10e8edb3657a307905e363d
"Kangding" respiratory pipeline (unsterilized)
TW: “康定”呼吸器管路(未滅菌)
Taiwan·Risk Class 1·COMDEK INDUSTRIAL CORPORATION·Registered Oct 04, 2012 – Oct 04, 2027ActiveRegistration details
- Analysis ID
- c92b721ba10e8edb3657a307905e363d
Company information
- Manufacturer
- COMDEK INDUSTRIAL CORPORATION
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- COMDEK INDUSTRIAL 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
- Domestic
Dates and status
- Registration Date
- Oct 04, 2012
- Expiry Date
- Oct 04, 2027
About this record
Access comprehensive regulatory information for "Kangding" respiratory pipeline (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number c92b721ba10e8edb3657a307905e363d and manufactured by COMDEK INDUSTRIAL CORPORATION. The authorized representative in Taiwan is COMDEK INDUSTRIAL CORPORATION.
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