Taiwan FDA registration fd365e48ad89387777a6b544c5e7e29a
"Roche" RNA Positive Control Probe (Non-sterile)
TW: "羅氏" 核糖核酸陽性品管探針(未滅菌)
Registration details
- Analysis ID
- fd365e48ad89387777a6b544c5e7e29a
- License Form
- Ministry of Health Medical Device Import No. 022987
- Customs Code
- DHA09402298704
Company information
- Manufacturer
- VENTANA MEDICAL SYSTEMS, INC.
- Manufacturer Country
- United States
- Authorized Representative
- ROCHE DIAGNOSTICS LTD.
Product details
- Intended Use
- Limited to the classification and grading management of medical equipment, quality control materials (analytical and non-analytical) (A.1660) the first level identification range.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A1660 Quality Control Materials (Analytical and Non-Analytical)
- Import Information
- Imported from abroad; GMP
Dates and status
- Registration Date
- Dec 21, 2022
- Expiry Date
- Dec 21, 2027
About this record
Access comprehensive regulatory information for "Roche" RNA Positive Control Probe (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 fd365e48ad89387777a6b544c5e7e29a and manufactured by VENTANA MEDICAL SYSTEMS, INC.. The authorized representative in Taiwan is ROCHE DIAGNOSTICS LTD..
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