Taiwan FDA registration 8b58e929a1c4413a31e2714403b8a7fb
"Synthetic" Fujitec controllable guide sheath
TW: “先健”富士達可控式導引鞘
Taiwan·Risk Class 2·LIFETECH SCIENTIFIC (SHENZHEN) CO., LTD·Registered Nov 17, 2011 – Nov 17, 2016CancelledRegistration details
- Analysis ID
- 8b58e929a1c4413a31e2714403b8a7fb
- Customs Code
- DHA04200040503
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.1250 Percutaneous catheters
- Import Information
- Input;; Chinese goods
Dates and status
- Registration Date
- Nov 17, 2011
- Expiry Date
- Nov 17, 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 "Synthetic" Fujitec controllable guide sheath in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 8b58e929a1c4413a31e2714403b8a7fb and manufactured by LIFETECH SCIENTIFIC (SHENZHEN) CO., LTD. The authorized representative in Taiwan is SHIUH-CHYNG MEDICAL CO., LTD..
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