Taiwan FDA registration e251f586e7356fad948b70a9240e96cd
"Medtronic" general purpose cassette
TW: "美敦力" 一般用途卡匣
Taiwan·Risk Class 2·MEDTRONIC PERFUSION SYSTEMS·Registered Mar 13, 2006 – Mar 13, 2011CancelledRegistration details
- Analysis ID
- e251f586e7356fad948b70a9240e96cd
- Customs Code
- DHA00601612503
Company information
- Manufacturer
- MEDTRONIC PERFUSION SYSTEMS
- Manufacturer Country
- United States
- Authorized Representative
- MEDTRONIC (TAIWAN) LTD.
Product details
- Intended Use
- With an automatic coagulation timer, the coagulation test endpoint of the coagulation reaction requiring recalcification is determined.
- Product Type (Level 1)
- B Hematology, pathology, and genetics
- Product Type (Level 2)
- B.5425 Versatile system for in vitro agglutination studies
- Import Information
- import
Dates and status
- Registration Date
- Mar 13, 2006
- Expiry Date
- Mar 13, 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" general purpose cassette in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e251f586e7356fad948b70a9240e96cd and manufactured by MEDTRONIC PERFUSION SYSTEMS. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) LTD..
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