Taiwan FDA registration b5dc4140f8c71b59effebed8d0831952
"Covidien" Kentley compression sleeve
TW: “柯惠”肯特利壓縮套
Taiwan·Risk Class 2·COVIDIEN LLC;; COVID·Registered Jan 07, 2013 – Jan 07, 2018CancelledRegistration details
- Analysis ID
- b5dc4140f8c71b59effebed8d0831952
- Customs Code
- DHA00602438502
Company information
- Manufacturer
- COVIDIEN LLC;; COVID
- Manufacturer Country
- United States
- Authorized Representative
- Taiwan Covidien Corporation Limited
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- E Cardiovascular Medicine Science
- Product Type (Level 2)
- E.5800 Compression sleeves for limbs
- Import Information
- import
Dates and status
- Registration Date
- Jan 07, 2013
- Expiry Date
- Jan 07, 2018
- Cancellation Date
- Mar 16, 2017
Cancellation information
- Status
- Logged out
- Reason
- 公司歇業
About this record
Access comprehensive regulatory information for "Covidien" Kentley compression sleeve in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number b5dc4140f8c71b59effebed8d0831952 and manufactured by COVIDIEN LLC;; COVID. The authorized representative in Taiwan is Taiwan Covidien Corporation Limited.
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