Taiwan FDA registration 2786ab17cca5f1a4b8092d4cb02c20cf
"New Guangye" laryngeal hood (sterilized)
TW: "新廣業" 喉頭罩 (滅菌)
Taiwan·Risk Class 1·Xubang Medical Equipment Co., Ltd·Registered Jan 09, 2007 – Jan 09, 2022CancelledRegistration details
- Analysis ID
- 2786ab17cca5f1a4b8092d4cb02c20cf
- Customs Code
- DHY04300175508
Company information
- Manufacturer
- Xubang Medical Equipment Co., Ltd
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- HSINER CO., LTD.
Product details
- Intended Use
- Limited to the first level recognition range of the oropharyngeal airway tube (D.5110) for the management of medical devices.
- Product Type (Level 1)
- D Anesthesiology
- Product Type (Level 2)
- D.5110 Oropharyngeal airway tubes
- Import Information
- Contract manufacturing
Dates and status
- Registration Date
- Jan 09, 2007
- Expiry Date
- Jan 09, 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 "New Guangye" laryngeal hood (sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 2786ab17cca5f1a4b8092d4cb02c20cf and manufactured by Xubang Medical Equipment Co., Ltd. The authorized representative in Taiwan is HSINER CO., LTD..
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