Taiwan FDA registration 20d5af56632e5f01802dea4c4f604d78
"Roche" Anti-Lambda Rabbit Multi-strain Primary Antibody Reagent (Non-sterilized)
TW: "羅氏" 抗Lambda 兔多株一級抗體試劑(未滅菌)
Taiwan·Risk Class 1·VENTANA MEDICAL SYSTEMS, INC.·Registered Aug 07, 2023 – Aug 07, 2028ActiveRegistration details
- Analysis ID
- 20d5af56632e5f01802dea4c4f604d78
- Customs Code
- DHA09402320008
Company information
- Manufacturer
- VENTANA MEDICAL SYSTEMS, INC.
- Manufacturer Country
- United States
- Authorized Representative
- ROCHE DIAGNOSTICS LTD.
Product details
- Intended Use
- Limit the classification and grading management of medical equipment "immunopathological histochemical reagents and sets (B.1860) the first level identification range.
- Product Type (Level 1)
- B Hematology, pathology, and genetics
- Product Type (Level 2)
- B.1860 Immunopathological histochemistry reagents and kits
- Import Information
- QMS/QSD;; 輸入
Dates and status
- Registration Date
- Aug 07, 2023
- Expiry Date
- Aug 07, 2028
About this record
Access comprehensive regulatory information for "Roche" Anti-Lambda Rabbit Multi-strain Primary Antibody Reagent (Non-sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 20d5af56632e5f01802dea4c4f604d78 and manufactured by VENTANA MEDICAL SYSTEMS, INC.. The authorized representative in Taiwan is ROCHE DIAGNOSTICS LTD..
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