Taiwan FDA registration 8e5ac967156da1d8189a847d0560709f
"Kenmax" Vacuum Powered Body Fluid Absorption Device (Sterilization)
TW: “肯麥司” 真空動力式體液吸收器具 (滅菌)
Taiwan·Risk Class 1·KENDALL KENMEX, A DIVISION OF, TYCO HEALTHCARE GROUP LP·Registered Dec 05, 2011 – Dec 05, 2016CancelledRegistration details
- Analysis ID
- 8e5ac967156da1d8189a847d0560709f
- Customs Code
- DHA04401113909
Company information
- Manufacturer Country
- Mexico
- Authorized Representative
- Taiwan Covidien Corporation Limited
Product details
- Intended Use
- Limited to the first level recognition range of the Measures for the Administration of Medical Devices "Vacuum-powered Body Fluid Absorption Devices (J.6740)".
- Product Type (Level 1)
- J General hospital and personal use equipment
- Product Type (Level 2)
- J.6740 Vacuum-powered fluid absorption apparatus
- Import Information
- QMS/QSD;; 輸入
Dates and status
- Registration Date
- Dec 05, 2011
- Expiry Date
- Dec 05, 2016
- Cancellation Date
- Mar 16, 2017
Cancellation information
- Status
- Logged out
- Reason
- 公司歇業
About this record
Access comprehensive regulatory information for "Kenmax" Vacuum Powered Body Fluid Absorption Device (Sterilization) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 8e5ac967156da1d8189a847d0560709f and manufactured by KENDALL KENMEX, A DIVISION OF, TYCO HEALTHCARE GROUP LP. The authorized representative in Taiwan is Taiwan Covidien Corporation Limited.
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