Taiwan FDA registration 583ef3bcd613a1829f444c150e891b8a
Mei Ariel Nyazi Parasite Test Kit (Unsterilized)
TW: 美艾利爾 揣耶濟 寄生蟲檢測套組(未滅菌)
Taiwan·Risk Class 1·ALERE SAN DIEGO, INC.·Registered Dec 10, 2010 – Dec 10, 2020CancelledRegistration details
- Analysis ID
- 583ef3bcd613a1829f444c150e891b8a
- Customs Code
- DHA04400965904
Company information
- Manufacturer
- ALERE SAN DIEGO, INC.
- Manufacturer Country
- United States
- Authorized Representative
- Abbott Rapid Diagnostics Health Corp.
Product details
- Intended Use
- Limited to the first level identification range of "Histolytic amoeba serum reagent (C.3220)" of the Measures for the Administration of Medical Devices.
- Product Type (Level 1)
- C Immunology and microbiology
- Product Type (Level 2)
- C.3220 痢疾阿米巴血清試劑
- Import Information
- import
Dates and status
- Registration Date
- Dec 10, 2010
- Expiry Date
- Dec 10, 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 Mei Ariel Nyazi Parasite Test Kit (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 583ef3bcd613a1829f444c150e891b8a and manufactured by ALERE SAN DIEGO, INC.. The authorized representative in Taiwan is Abbott Rapid Diagnostics Health Corp..
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