Taiwan FDA registration 0c0d8cf8dc4888f7e96b61bdd4ee9ba5
"Jisheng" endotracheal probe (unsterilized)
TW: “吉生” 氣管內管探針 (未滅菌)
Taiwan·Risk Class 1·JI SHENG MEDICAL COMPANY LIMITED·Registered Apr 12, 2022 – Apr 12, 2027ActiveRegistration details
- Analysis ID
- 0c0d8cf8dc4888f7e96b61bdd4ee9ba5
Company information
- Manufacturer
- JI SHENG MEDICAL COMPANY LIMITED
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- JI SHENG MEDICAL COMPANY LIMITED
Product details
- Intended Use
- Limited to the first level identification range of the "endotracheal tube probe (D.5790)" of the Measures for the Classification and Grading Management of Medical Equipment.
- Product Type (Level 1)
- D Anesthesiology
- Product Type (Level 2)
- D.5790 氣管內管探針
- Import Information
- 國產;; QMS/QSD
Dates and status
- Registration Date
- Apr 12, 2022
- Expiry Date
- Apr 12, 2027
About this record
Access comprehensive regulatory information for "Jisheng" endotracheal probe (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 0c0d8cf8dc4888f7e96b61bdd4ee9ba5 and manufactured by JI SHENG MEDICAL COMPANY LIMITED. The authorized representative in Taiwan is JI SHENG MEDICAL COMPANY LIMITED.
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