Taiwan FDA registration e1442461b6b73bb5017fde8efc738b89
“OMRON” Mesh Nebulizer
TW: “歐姆龍”網眼式噴霧器
Taiwan·Risk Class 2·MD·OMRON HEALTHCARE CO., LTD. MATSUSAKA FACTORY·Registered Mar 26, 2019 – Mar 26, 2024ExpiredRegistration details
- Analysis ID
- e1442461b6b73bb5017fde8efc738b89
- License Form
- Ministry of Health Medical Device Import No. 032313
- Customs Code
- DHA05603231302
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
- Mar 26, 2019
- Expiry Date
- Mar 26, 2024
About this record
Access comprehensive regulatory information for “OMRON” Mesh Nebulizer in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e1442461b6b73bb5017fde8efc738b89 and manufactured by OMRON HEALTHCARE CO., LTD. MATSUSAKA FACTORY. The authorized representative in Taiwan is OMRON HEALTHCARE TAIWAN CO., LTD..
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