Taiwan FDA registration 767feb8ea3a252a14a5e0fb9010db155
ProSpecT Entamoeba histolytica Microplate Assay (Non-Sterile)
TW: “銳邁” 痢疾阿米巴檢測試劑(未滅菌)
Taiwan·Risk Class 1·MD·OXOID LTD·Registered Dec 31, 2019 – Dec 31, 2024ExpiredRegistration details
- Analysis ID
- 767feb8ea3a252a14a5e0fb9010db155
- License Form
- Ministry of Health Medical Device Import No. 021153
- Customs Code
- DHA09402115302
Company information
- Manufacturer
- OXOID LTD
- Manufacturer Country
- United Kingdom
- Authorized Representative
- CREATIVE LIFE SCIENCE CO., LTD.
Product details
- Intended Use
- Limited to the first level identification range of the Measures for the Administration of Medical Devices "Dysentery Amoeba Sera Reagent (C.3220)".
- Product Type (Level 1)
- C Immunology and microbiology devices
- Product Type (Level 2)
- C3220 Dysentery amoeba serum reagent
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Dec 31, 2019
- Expiry Date
- Dec 31, 2024
About this record
Access comprehensive regulatory information for ProSpecT Entamoeba histolytica Microplate Assay (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 767feb8ea3a252a14a5e0fb9010db155 and manufactured by OXOID LTD. The authorized representative in Taiwan is CREATIVE LIFE SCIENCE CO., LTD..
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