Taiwan FDA registration 0ffadcbc7a6811fa999fb17e19ae711f
"Kemel" drug sealed closed infusion sleeve
TW: “可美爾”藥封密閉式輸液套
Taiwan·Risk Class 2·CARMEL PHARMA AB·Registered May 27, 2010 – May 27, 2015CancelledRegistration details
- Analysis ID
- 0ffadcbc7a6811fa999fb17e19ae711f
- Customs Code
- DHA00602106100
Company information
- Manufacturer
- CARMEL PHARMA AB
- Manufacturer Country
- Sweden
- Authorized Representative
- MEDFRONT MEDICAL TECHNOLOGY CORPORATION
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- J General hospital and personal use equipment
- Product Type (Level 2)
- J.5440 血管內輸液套
- Import Information
- import
Dates and status
- Registration Date
- May 27, 2010
- Expiry Date
- May 27, 2015
- Cancellation Date
- Jul 02, 2018
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Kemel" drug sealed closed infusion sleeve in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 0ffadcbc7a6811fa999fb17e19ae711f and manufactured by CARMEL PHARMA AB. The authorized representative in Taiwan is MEDFRONT MEDICAL TECHNOLOGY CORPORATION.
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