Taiwan FDA registration 297c7fa14beb4c7c45a48f03f1f575df
"Omron" handheld inhaler (unsterilized)
TW: "歐姆龍" 手持吸入器(未滅菌)
Registration details
- Analysis ID
- 297c7fa14beb4c7c45a48f03f1f575df
- Customs Code
- DHA09600475803
Company information
- Manufacturer Country
- Japan;;China
- Authorized Representative
- OMRON HEALTHCARE TAIWAN CO., LTD.
Product details
- Intended Use
- This product is only suitable for humidifying and washing the nasal cavity and throat to improve discomfort.
- Product Type (Level 1)
- G ENT Science
- Product Type (Level 2)
- G.9999 Miscellaneous
- Import Information
- QMS/QSD;; Input;; Chinese goods
Dates and status
- Registration Date
- Mar 29, 2023
- Expiry Date
- Mar 29, 2028
About this record
Access comprehensive regulatory information for "Omron" handheld inhaler (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 297c7fa14beb4c7c45a48f03f1f575df and manufactured by OMRON DALIAN CO., LTD.;; OMRON HEALTHCARE CO., LTD.. The authorized representative in Taiwan is OMRON HEALTHCARE TAIWAN CO., LTD..
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