Taiwan FDA registration 4a8549c5ecf8e90ee376b090a655d21f
"Ruisheng" atomizer
TW: “瑞盛”霧化器
Taiwan·Risk Class 2·Shangyue Technology Co., Ltd. factory·Registered Jun 21, 2013 – Jun 01, 2021CancelledRegistration details
- Analysis ID
- 4a8549c5ecf8e90ee376b090a655d21f
Company information
- Manufacturer
- Shangyue Technology Co., Ltd. factory
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- ROSSMAX INNOTEK CORP.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- D Anesthesiology
- Product Type (Level 2)
- D.5630 Nebulizer
- Import Information
- Domestic;; Contract manufacturing
Dates and status
- Registration Date
- Jun 21, 2013
- Expiry Date
- Jun 01, 2021
- Cancellation Date
- Sep 23, 2023
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for "Ruisheng" atomizer in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 4a8549c5ecf8e90ee376b090a655d21f and manufactured by Shangyue Technology Co., Ltd. factory. The authorized representative in Taiwan is ROSSMAX INNOTEK CORP..
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