Taiwan FDA registration 0d79cbe344f1f7214118b332d38bc904
"Xianjian" vena cava filter
TW: “先健”腔靜脈過濾器
Taiwan·Risk Class 2·LIFETECH SCIENTIFIC (SHENZHEN) CO., LTD·Registered Dec 21, 2011 – Dec 21, 2016CancelledRegistration details
- Analysis ID
- 0d79cbe344f1f7214118b332d38bc904
- Customs Code
- DHA04200032202
Company information
- Manufacturer
- LIFETECH SCIENTIFIC (SHENZHEN) CO., LTD
- Manufacturer Country
- China
- Authorized Representative
- SHIUH-CHYNG MEDICAL CO., LTD.
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.4260 Cardiopulmonary vascular bypass artery blood spiller
- Import Information
- Chinese goods;; input
Dates and status
- Registration Date
- Dec 21, 2011
- Expiry Date
- Dec 21, 2016
- Cancellation Date
- Aug 14, 2018
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Xianjian" vena cava filter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 0d79cbe344f1f7214118b332d38bc904 and manufactured by LIFETECH SCIENTIFIC (SHENZHEN) CO., LTD. The authorized representative in Taiwan is SHIUH-CHYNG MEDICAL CO., LTD..
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