Taiwan FDA registration 814e67a3d066792f0f43068e08a7e32e
“Surefire” Infusion System
TW: “旭發”輸液系統
Taiwan·Risk Class 2·MD·Surefire Medical, Inc.·Registered Oct 31, 2013 – Oct 31, 2018CancelledRegistration details
- Analysis ID
- 814e67a3d066792f0f43068e08a7e32e
- License Form
- Ministry of Health Medical Device Import No. 025444
- Customs Code
- DHA05602544400
Company information
- Manufacturer
- Surefire Medical, Inc.
- Manufacturer Country
- United States
- Authorized Representative
- CEMMA MEDICAL CO., LTD.
Product details
- Product Type (Level 1)
- E Cardiovascular devices
- Product Type (Level 2)
- E1200 Diagnostic endovascular catheter
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Oct 31, 2013
- Expiry Date
- Oct 31, 2018
- Cancellation Date
- Aug 05, 2022
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for “Surefire” Infusion System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 814e67a3d066792f0f43068e08a7e32e and manufactured by Surefire Medical, Inc.. The authorized representative in Taiwan is CEMMA MEDICAL CO., LTD..
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