Taiwan FDA registration a296d8b6b217e54d345a6fb66e8fa740
Correction solution for heme detection in San Tino stool
TW: 聖堤諾便中血紅素檢測校正液
Taiwan·Risk Class 2·SENTINEL CH. S.p.A.·Registered Nov 25, 2020 – Nov 25, 2025ExpiredRegistration details
- Analysis ID
- a296d8b6b217e54d345a6fb66e8fa740
- Customs Code
- DHA05603416102
Company information
- Manufacturer
- SENTINEL CH. S.p.A.
- Manufacturer Country
- Italy
- Authorized Representative
- MEDTRI CO., LTD.
Product details
- Intended Use
- This product is paired with FOB Gold immunoturbidimetric analysis reagent to create a correction curve for the determination of heme in human feces.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1150 Calibrated Products
- Import Information
- Input;; QMS/QSD
Dates and status
- Registration Date
- Nov 25, 2020
- Expiry Date
- Nov 25, 2025
About this record
Access comprehensive regulatory information for Correction solution for heme detection in San Tino stool in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number a296d8b6b217e54d345a6fb66e8fa740 and manufactured by SENTINEL CH. S.p.A.. The authorized representative in Taiwan is MEDTRI CO., LTD..
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