Taiwan FDA registration bee9431a2f5a2f5bb3bae842bf6a8ffb
"Invivoscribe" Clonal Control DNA and RNA (Non-sterile)
TW: 〝因我快〞核酸檢測對照組(未滅菌)
Registration details
- Analysis ID
- bee9431a2f5a2f5bb3bae842bf6a8ffb
- License Form
- Ministry of Health Medical Device Import No. 022961
- Customs Code
- DHA09402296102
Company information
- Manufacturer
- Invivoscribe Inc.
- Manufacturer Country
- United States
- Authorized Representative
- BOND BIOTECH, INC.
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
Dates and status
- Registration Date
- Nov 24, 2022
- Expiry Date
- Nov 24, 2027
About this record
Access comprehensive regulatory information for "Invivoscribe" Clonal Control DNA and RNA (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 bee9431a2f5a2f5bb3bae842bf6a8ffb and manufactured by Invivoscribe Inc.. The authorized representative in Taiwan is BOND BIOTECH, INC..
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