Taiwan FDA registration 3b043c5bf952885b9fc67f40f14d2ce5
"SENSONICS" Olfactory test device (Non-Sterile)
TW: "森嵩尼克斯"嗅覺測試裝置 (未滅菌)
Taiwan·Risk Class 1·MD·SENSONICS INTERNATIONAL·Registered Oct 19, 2018 – Oct 19, 2023ExpiredRegistration details
- Analysis ID
- 3b043c5bf952885b9fc67f40f14d2ce5
- License Form
- Ministry of Health Medical Device Import No. 019716
- Customs Code
- DHA09401971602
Company information
- Manufacturer
- SENSONICS INTERNATIONAL
- Manufacturer Country
- United States
- Authorized Representative
- WHOLE WELL CO., LTD.
Product details
- Intended Use
- Limited to the first level identification range of the "olfactory test device (G.1600)" of the Measures for the Administration of Medical Devices.
- Product Type (Level 1)
- G ENT device
- Product Type (Level 2)
- G1600 olfactory test device
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Oct 19, 2018
- Expiry Date
- Oct 19, 2023
About this record
Access comprehensive regulatory information for "SENSONICS" Olfactory test device (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 3b043c5bf952885b9fc67f40f14d2ce5 and manufactured by SENSONICS INTERNATIONAL. The authorized representative in Taiwan is WHOLE WELL CO., LTD..
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