Taiwan FDA registration 52e3d0fe4e62f57f0b1e42d27058d8ef
"Hongan" endotracheal probe (unsterilized)
TW: "宏安" 氣管內管探針 (未滅菌)
Taiwan·Risk Class 1·HONG AN MEDICAL APPLIANCE CO., LTD.·Registered Mar 06, 2012 – Mar 06, 2022CancelledRegistration details
- Analysis ID
- 52e3d0fe4e62f57f0b1e42d27058d8ef
- Customs Code
- DHA04600160002
Company information
- Manufacturer
- HONG AN MEDICAL APPLIANCE CO., LTD.
- Manufacturer Country
- China
- Authorized Representative
- SHAN-LUEN MEDICAL CO., LTD.
Product details
- Intended Use
- Limited to the first level recognition range of endotracheal tube probe (D.5790) of the management method for medical equipment.
- Product Type (Level 1)
- D Anesthesiology
- Product Type (Level 2)
- D.5790 氣管內管探針
- Import Information
- Input;; Chinese goods
Dates and status
- Registration Date
- Mar 06, 2012
- Expiry Date
- Mar 06, 2022
- Cancellation Date
- Apr 12, 2024
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Hongan" 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 52e3d0fe4e62f57f0b1e42d27058d8ef and manufactured by HONG AN MEDICAL APPLIANCE CO., LTD.. The authorized representative in Taiwan is SHAN-LUEN MEDICAL CO., LTD..
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