Taiwan FDA registration e1bd6771362b5f5f93623bb6416df3ff
“Lorne” Anti-M Polyclonal
TW: “羅倫”多株抗體抗M血清
Taiwan·Risk Class 2·MD·Lorne Laboratories Limited·Registered Nov 20, 2018 – Nov 20, 2028ActiveRegistration details
- Analysis ID
- e1bd6771362b5f5f93623bb6416df3ff
- License Form
- Ministry of Health Medical Device Import No. 031802
- Customs Code
- DHA05603180202
Company information
- Manufacturer
- Lorne Laboratories Limited
- Manufacturer Country
- United Kingdom
- Authorized Representative
- GLORY BIOSCIENCE CO., LTD.
Product details
- Intended Use
- Appraisal M blood type fraction.
- Product Type (Level 1)
- B Hematology and pathology devices
- Product Type (Level 2)
- B4020 Analyze specific reagents
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Nov 20, 2018
- Expiry Date
- Nov 20, 2028
About this record
Access comprehensive regulatory information for “Lorne” Anti-M Polyclonal in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e1bd6771362b5f5f93623bb6416df3ff and manufactured by Lorne Laboratories Limited. The authorized representative in Taiwan is GLORY BIOSCIENCE CO., LTD..
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