Taiwan FDA registration b71155cce9909386f86121a58f5c5f88
Pressure device for "Prowei" blood transfusion bag (unsterilized)
TW: “普威”輸血袋用壓力器 (未滅菌)
Taiwan·Risk Class 1·KAIWEI (SHENZHEN) CO., LTD.·Registered Dec 25, 2008 – Dec 25, 2013CancelledRegistration details
- Analysis ID
- b71155cce9909386f86121a58f5c5f88
- Customs Code
- DHA04600061902
Company information
- Manufacturer
- KAIWEI (SHENZHEN) CO., LTD.
- Manufacturer Country
- China
- Authorized Representative
- Proway International Limited
Product details
- Intended Use
- Limited to the first level identification range of pressure device for blood transfusion bag (J.5420) of the management method for medical equipment.
- Product Type (Level 1)
- J General hospital and personal use equipment
- Product Type (Level 2)
- J.5420 靜脈輸液袋用壓力器
- Import Information
- Input;; Chinese goods
Dates and status
- Registration Date
- Dec 25, 2008
- Expiry Date
- Dec 25, 2013
- Cancellation Date
- Jun 17, 2015
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for Pressure device for "Prowei" blood transfusion 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 b71155cce9909386f86121a58f5c5f88 and manufactured by KAIWEI (SHENZHEN) CO., LTD.. The authorized representative in Taiwan is Proway International Limited.
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