Taiwan FDA registration 294f20ac60a963036794d2b6fec5d38f
"Fentith" Hot and Cold Compress Bag (Unsterilized)
TW: “芬蒂思”冷熱敷袋 (未滅菌)
Registration details
- Analysis ID
- 294f20ac60a963036794d2b6fec5d38f
Company information
- Manufacturer
- CHENG HOUSE ENTERPRISE CO., LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- FANTASY INDUSTRY CO., LTD.
Product details
- Intended Use
- It is limited to the scope of the first level of identification of the medical equipment management measures "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
- Contract manufacturing;; Domestic
Dates and status
- Registration Date
- Apr 27, 2006
- Expiry Date
- Apr 27, 2011
- Cancellation Date
- Nov 23, 2012
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Fentith" Hot and Cold Compress Bag (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 294f20ac60a963036794d2b6fec5d38f and manufactured by CHENG HOUSE ENTERPRISE CO., LTD.. The authorized representative in Taiwan is FANTASY INDUSTRY CO., LTD..
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