Taiwan FDA registration dfb4ac106a09ae1303c9fec501dcfffe
"Jiachuang" oropharyngeal airway tube (unsterilized)
TW: “佳創”口咽氣道管 (未滅菌)
Taiwan·Risk Class 1·Longtan Factory of Jiachuang Biotechnology Co., Ltd·Registered Jan 10, 2020 – Jan 10, 2030ActiveRegistration details
- Analysis ID
- dfb4ac106a09ae1303c9fec501dcfffe
Company information
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- CREATE BIOTECH CO., LTD.
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;; 國產
Dates and status
- Registration Date
- Jan 10, 2020
- Expiry Date
- Jan 10, 2030
About this record
Access comprehensive regulatory information for "Jiachuang" oropharyngeal airway tube (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number dfb4ac106a09ae1303c9fec501dcfffe and manufactured by Longtan Factory of Jiachuang Biotechnology Co., Ltd. The authorized representative in Taiwan is CREATE BIOTECH CO., LTD..
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