Taiwan FDA registration cb22c27c5ee5504d69d3c9a65128369f
“ Elitech” Erythrocyte Sedimentation Rate Test (Non-Sterile)
TW: “艾利鐵克” 紅血球沉澱速率試驗(未滅菌)
Taiwan·Risk Class 1·MD·ELITechGroup B.V.·Registered Mar 02, 2015 – Mar 02, 2020CancelledRegistration details
- Analysis ID
- cb22c27c5ee5504d69d3c9a65128369f
- License Form
- Ministry of Health Medical Device Import No. 014952
- Customs Code
- DHA09401495202
Company information
- Manufacturer
- ELITechGroup B.V.
- Manufacturer Country
- Netherlands
- Authorized Representative
- Yuxing Enterprise Co., Ltd
Product details
- Product Type (Level 1)
- B Hematology and pathology devices
- Product Type (Level 2)
- B6700 Red blood cell sedimentation rate test
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Mar 02, 2015
- Expiry Date
- Mar 02, 2020
- Cancellation Date
- Jul 15, 2022
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for “ Elitech” Erythrocyte Sedimentation Rate Test (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number cb22c27c5ee5504d69d3c9a65128369f and manufactured by ELITechGroup B.V.. The authorized representative in Taiwan is Yuxing Enterprise Co., Ltd.
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