Taiwan FDA registration 42262afed213d9529c2a66c0d0bb69ee
“Techno-path”Multichem IA Plus
TW: “泰可諾” 多項目免疫分析品管液
Taiwan·Risk Class 2·MD·TECHNO-PATH MANUFACTURING LTD·Registered May 10, 2019 – May 10, 2024ExpiredRegistration details
- Analysis ID
- 42262afed213d9529c2a66c0d0bb69ee
- License Form
- Ministry of Health Medical Device Import No. 032430
- Customs Code
- DHA05603243006
Company information
- Manufacturer
- TECHNO-PATH MANUFACTURING LTD
- Manufacturer Country
- Ireland
- Authorized Representative
- ABBOTT LABORATORIES SERVICES LLC TAIWAN BRANCH (U.S.A.)
Product details
- Intended Use
- This product can be used as an analysed mass management serum to monitor the precision of laboratory testing procedures for the analytes listed in this specification.
- 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
- May 10, 2019
- Expiry Date
- May 10, 2024
About this record
Access comprehensive regulatory information for “Techno-path”Multichem IA Plus in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 42262afed213d9529c2a66c0d0bb69ee and manufactured by TECHNO-PATH MANUFACTURING LTD. The authorized representative in Taiwan is ABBOTT LABORATORIES SERVICES LLC TAIWAN BRANCH (U.S.A.).
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