Taiwan FDA registration 573a0c2a126fcb0e6a25be432dcc229d
"Aon" laryngeal mask (sterilized)
TW: “怡安” 喉罩(滅菌)
Taiwan·Risk Class 1·BenQ Sanfeng Medical Equipment Co., Ltd. Taichung Factory;; Aon Medical Devices Co., Ltd·Registered Jul 08, 2020 – Jul 08, 2025ExpiredRegistration details
- Analysis ID
- 573a0c2a126fcb0e6a25be432dcc229d
Company information
- Manufacturer
- BenQ Sanfeng Medical Equipment Co., Ltd. Taichung Factory;; Aon Medical Devices Co., Ltd
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- LILY MEDICAL CORPORATION
Product details
- Intended Use
- Limited to the classification and grading management method of medical equipment, oropharyngeal airway canal (D.5110) first grade identification range.
- Product Type (Level 1)
- D Anesthesiology
- Product Type (Level 2)
- D.5110 Oropharyngeal airway tubes
- Import Information
- QMS/QSD;; 委託製造;; 國產
Dates and status
- Registration Date
- Jul 08, 2020
- Expiry Date
- Jul 08, 2025
About this record
Access comprehensive regulatory information for "Aon" laryngeal mask (sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 573a0c2a126fcb0e6a25be432dcc229d and manufactured by BenQ Sanfeng Medical Equipment Co., Ltd. Taichung Factory;; Aon Medical Devices Co., Ltd. The authorized representative in Taiwan is LILY MEDICAL CORPORATION.
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