Taiwan FDA registration c0c3cf844038eb8343e29c05aad545a1
"Remon" fibrin/fibrinogen lysate detection kit
TW: "銳盟" 纖維蛋白/纖維蛋白原裂解產物檢測套組
Taiwan·Risk Class 2·REMEL EUROPE LIMITED·Registered Feb 09, 2006 – Feb 09, 2016CancelledRegistration details
- Analysis ID
- c0c3cf844038eb8343e29c05aad545a1
- Customs Code
- DHA00601597802
Company information
- Manufacturer
- REMEL EUROPE LIMITED
- Manufacturer Country
- United Kingdom
- Authorized Representative
- SCN TRADING COMPANY LIMITED
Product details
- Intended Use
- Rapid semi-quantitative determination of fibrin/fibrinogen cleavage products (FDP) in human serum and urine samples.
- Product Type (Level 1)
- B Hematology, pathology, and genetics
- Product Type (Level 2)
- B.7320 Fibrinogen/Fibrinolysis Product Analysis
- Import Information
- import
Dates and status
- Registration Date
- Feb 09, 2006
- Expiry Date
- Feb 09, 2016
- Cancellation Date
- Jan 20, 2017
Cancellation information
- Status
- Logged out
- Reason
- 申復經核不准
About this record
Access comprehensive regulatory information for "Remon" fibrin/fibrinogen lysate detection kit in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number c0c3cf844038eb8343e29c05aad545a1 and manufactured by REMEL EUROPE LIMITED. The authorized representative in Taiwan is SCN TRADING COMPANY LIMITED.
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