Taiwan FDA registration 38143ca40ebf63f09e88481100ce4867
“Sysmex” Revohem Ristocetin
TW: “希森美康”瑞斯特黴素檢測試劑
Taiwan·Risk Class 2·MD·HYPHEN BioMed·Registered Dec 19, 2018 – Dec 19, 2028ActiveRegistration details
- Analysis ID
- 38143ca40ebf63f09e88481100ce4867
- License Form
- Ministry of Health Medical Device Import No. 031972
- Customs Code
- DHA05603197201
Company information
- Manufacturer
- HYPHEN BioMed
- Manufacturer Country
- France
- Authorized Representative
- SYSMEX TAIWAN CO., LTD.
Product details
- Intended Use
- This product is used for the detection of platelet agglutination.
- Product Type (Level 1)
- B Hematology and pathology devices
- Product Type (Level 2)
- B5700 Automated platelet agglutination system
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Dec 19, 2018
- Expiry Date
- Dec 19, 2028
About this record
Access comprehensive regulatory information for “Sysmex” Revohem Ristocetin in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 38143ca40ebf63f09e88481100ce4867 and manufactured by HYPHEN BioMed. The authorized representative in Taiwan is SYSMEX TAIWAN CO., LTD..
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