Taiwan FDA registration 98040d2b0491b2c6dc9a09edf19f9255
"Medtronic" Hamilis heparin test cassette
TW: "美敦力" 漢密思肝素試驗卡匣
Taiwan·Risk Class 2·MEDTRONIC PERFUSION SYSTEMS·Registered Jun 27, 2006 – Jun 27, 2011CancelledRegistration details
- Analysis ID
- 98040d2b0491b2c6dc9a09edf19f9255
- Customs Code
- DHA00601715606
Company information
- Manufacturer
- MEDTRONIC PERFUSION SYSTEMS
- Manufacturer Country
- United States
- Authorized Representative
- MEDTRONIC (TAIWAN) LTD.
Product details
- Intended Use
- It is a device for measuring the heparin content in the blood, and the patient is monitored and controlled for hemostasis.
- Product Type (Level 1)
- B Hematology, pathology, and genetics
- Product Type (Level 2)
- B.7525 Heparin analysis
- Import Information
- import
Dates and status
- Registration Date
- Jun 27, 2006
- Expiry Date
- Jun 27, 2011
- Cancellation Date
- Nov 06, 2012
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Medtronic" Hamilis heparin test cassette in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 98040d2b0491b2c6dc9a09edf19f9255 and manufactured by MEDTRONIC PERFUSION SYSTEMS. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) LTD..
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