Taiwan FDA registration db25ec0257153909745b4f07c3814f62
“Da Chung” Humidification Chamber
TW: “大中”加溫加濕瓶
Taiwan·Risk Class 2·MD·Dazhong Medical Equipment Co., Ltd. Dongshan No. 2 Factory·Registered May 18, 2017 – May 18, 2027ActiveRegistration details
- Analysis ID
- db25ec0257153909745b4f07c3814f62
- License Form
- Ministry of Health Medical Device Manufacturing No. 005764
Company information
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- Dazhong Medical Equipment Co., Ltd. Dongshan No. 2 Factory
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)
- D5450 Gas humidifier for respirators
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- May 18, 2017
- Expiry Date
- May 18, 2027
About this record
Access comprehensive regulatory information for “Da Chung” Humidification Chamber in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number db25ec0257153909745b4f07c3814f62 and manufactured by Dazhong Medical Equipment Co., Ltd. Dongshan No. 2 Factory. The authorized representative in Taiwan is Dazhong Medical Equipment Co., Ltd. Dongshan No. 2 Factory.
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