Taiwan FDA registration 35f9dcdcb4d084396a0d3347e51f8fa9
"Jingxuan" flexible laryngoscope (unsterilized)
TW: "敬煇" 可彎曲式喉頭鏡 (未滅菌)
Taiwan·Risk Class 1·TAIEX CO., LTD.·Registered Feb 05, 2015 – Feb 05, 2020CancelledRegistration details
- Analysis ID
- 35f9dcdcb4d084396a0d3347e51f8fa9
Company information
- Manufacturer
- TAIEX CO., LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- TAIEX CO., LTD.
Product details
- Intended Use
- Limited to the first level of identification range of "Flexible Laryngoscope (D.5530)" under the Measures for the Administration of Medical Devices.
- Product Type (Level 1)
- D Anesthesiology
- Product Type (Level 2)
- D.5530 Curved laryngeal lenses
- Import Information
- Domestic
Dates and status
- Registration Date
- Feb 05, 2015
- Expiry Date
- Feb 05, 2020
- Cancellation Date
- Oct 17, 2019
Cancellation information
- Status
- Logged out
- Reason
- 自請註銷
About this record
Access comprehensive regulatory information for "Jingxuan" flexible laryngoscope (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 35f9dcdcb4d084396a0d3347e51f8fa9 and manufactured by TAIEX CO., LTD.. The authorized representative in Taiwan is TAIEX CO., LTD..
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