Taiwan FDA registration 0ec93aa724fa7834de9a3a67021cfb20
"Roche" cobas Liat Strep A (Non-Sterile)
TW: "羅氏"可霸斯萊特A型鏈球菌快速檢驗試劑(未滅菌)
Registration details
- Analysis ID
- 0ec93aa724fa7834de9a3a67021cfb20
- License Form
- Ministry of Health Medical Device Import No. 018417
- Customs Code
- DHA09401841700
Company information
- Manufacturer
- ROCHE MOLECULAR SYSTEMS, INC.
- Manufacturer Country
- United States
- Authorized Representative
- ROCHE DIAGNOSTICS LTD.
Product details
- Intended Use
- Restriction of medical device management methods Streptococcus belongs to the first level identification range of serum reagent (C.3740).
- Product Type (Level 1)
- C Immunology and microbiology devices
- Product Type (Level 2)
- C3740 Streptococcus serology
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Oct 17, 2017
- Expiry Date
- Oct 17, 2022
About this record
Access comprehensive regulatory information for "Roche" cobas Liat Strep A (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 0ec93aa724fa7834de9a3a67021cfb20 and manufactured by ROCHE MOLECULAR SYSTEMS, INC.. The authorized representative in Taiwan is ROCHE DIAGNOSTICS LTD..
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