Taiwan FDA registration 4ea92a73d3cdb5db4886f927deac06e8
"Desheng" cold compress (unsterilized)
TW: “得生”冷敷貼(未滅菌)
Taiwan·Risk Class 1·Desheng Pharmaceutical Co., Ltd. Plant 2·Registered Jun 16, 2011 – Jun 16, 2026CancelledRegistration details
- Analysis ID
- 4ea92a73d3cdb5db4886f927deac06e8
Company information
- Manufacturer
- Desheng Pharmaceutical Co., Ltd. Plant 2
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- Desheng Pharmaceutical Co., Ltd. Plant 2
Product details
- Intended Use
- Limited to the first level identification range of the Measures for the Administration of Medical Equipment "Medical Cold Compress Pack (O.5700)".
- Product Type (Level 1)
- o Physical Medical Sciences
- Product Type (Level 2)
- O.5700 醫療用冷熱敷裝置
- Import Information
- Domestic
Dates and status
- Registration Date
- Jun 16, 2011
- Expiry Date
- Jun 16, 2026
- Cancellation Date
- Sep 30, 2021
Cancellation information
- Status
- Logged out
- Reason
- 轉為登錄字號
About this record
Access comprehensive regulatory information for "Desheng" cold compress (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 4ea92a73d3cdb5db4886f927deac06e8 and manufactured by Desheng Pharmaceutical Co., Ltd. Plant 2. The authorized representative in Taiwan is Desheng Pharmaceutical Co., Ltd. Plant 2.
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