Taiwan FDA registration 1ac41a48c959123fd57d0c56eb4b10c2
“OMRON” UltraSonic Nebulizer
TW: “歐姆龍” 超音波噴霧治療器
Taiwan·Risk Class 2·MD·OMRON HEALTHCARE CO., LTD. MATSUSAKA FACTORY·Registered Apr 21, 2017 – Apr 21, 2027ActiveRegistration details
- Analysis ID
- 1ac41a48c959123fd57d0c56eb4b10c2
- License Form
- Ministry of Health Medical Device Import No. 029670
- Customs Code
- DHA05602967003
Company information
- Manufacturer
- OMRON HEALTHCARE CO., LTD. MATSUSAKA FACTORY
- Manufacturer Country
- Japan
- Authorized Representative
- OMRON HEALTHCARE TAIWAN CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- D Devices for anesthesiology
- Product Type (Level 2)
- D5630 Sprayer
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Apr 21, 2017
- Expiry Date
- Apr 21, 2027
About this record
Access comprehensive regulatory information for “OMRON” UltraSonic Nebulizer in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 1ac41a48c959123fd57d0c56eb4b10c2 and manufactured by OMRON HEALTHCARE CO., LTD. MATSUSAKA FACTORY. The authorized representative in Taiwan is OMRON HEALTHCARE TAIWAN CO., LTD..
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