Taiwan FDA registration 3678c100709c8b0a3aa666b6f5146407
"ZTE" nasal expander (unsterilized)
TW: "中興" 鼻腔擴大器 (未滅菌)
Taiwan·Risk Class 1·Shengyuan Instrument Co., Ltd. Taoyuan Factory·Registered Oct 09, 2018 – Oct 09, 2023ExpiredRegistration details
- Analysis ID
- 3678c100709c8b0a3aa666b6f5146407
Company information
- Manufacturer
- Shengyuan Instrument Co., Ltd. Taoyuan Factory
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- ZTE Medical Equipment Line
Product details
- Intended Use
- Limited to the first level identification range of the "nasal expander (G.3900)" of the classification and grading management method for medical devices.
- Product Type (Level 1)
- G ENT Science
- Product Type (Level 2)
- G.3900 Nasal extenders
- Import Information
- Contract manufacturing;; Domestic
Dates and status
- Registration Date
- Oct 09, 2018
- Expiry Date
- Oct 09, 2023
About this record
Access comprehensive regulatory information for "ZTE" nasal expander (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 3678c100709c8b0a3aa666b6f5146407 and manufactured by Shengyuan Instrument Co., Ltd. Taoyuan Factory. The authorized representative in Taiwan is ZTE Medical Equipment Line.
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