Taiwan FDA registration 9991a1f9e81f7171a9751848d8e9d283
"Elkafort" one-time laryngoscope blade (sterilized)
TW: “艾爾卡福特”一次使用型喉頭鏡葉片 (滅菌)
Taiwan·Risk Class 1·Xubang Medical Equipment Co., Ltd·Registered Jul 02, 2013 – Jul 02, 2023CancelledRegistration details
- Analysis ID
- 9991a1f9e81f7171a9751848d8e9d283
Company information
- Manufacturer
- Xubang Medical Equipment Co., Ltd
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- Xubang Medical Equipment Co., Ltd
Product details
- Intended Use
- Limited to the first level of identification scope of the Measures for the Administration of Medical Devices "Rigid Laryngoscopy (D.5540)".
- Product Type (Level 1)
- D Anesthesiology
- Product Type (Level 2)
- D.5540 Rigid laryngoscope
- Import Information
- 國產;; QMS/QSD
Dates and status
- Registration Date
- Jul 02, 2013
- Expiry Date
- Jul 02, 2023
- Cancellation Date
- Apr 08, 2019
Cancellation information
- Status
- Logged out
- Reason
- 自請註銷
About this record
Access comprehensive regulatory information for "Elkafort" one-time laryngoscope blade (sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 9991a1f9e81f7171a9751848d8e9d283 and manufactured by Xubang Medical Equipment Co., Ltd. The authorized representative in Taiwan is Xubang Medical Equipment Co., Ltd.
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