Taiwan FDA registration 651d3c47ca2e397dcb1c50a31fc640ed
“Techno-path” Multichem S Plus (Assayed)
TW: “泰可諾” 多項目生化分析血清品管液(已分析)
Taiwan·Risk Class 2·MD·TECHNO-PATH MANUFACTURING LTD·Registered Nov 11, 2014 – Nov 11, 2024ExpiredRegistration details
- Analysis ID
- 651d3c47ca2e397dcb1c50a31fc640ed
- License Form
- Ministry of Health Medical Device Import No. 026738
- Customs Code
- DHA05602673809
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
- Multichem S Plus (assayed) can be used as a third-party quality control serum to monitor the precision of the analytes contained in the replica sheet in laboratory testing procedures.
- 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 11, 2014
- Expiry Date
- Nov 11, 2024
About this record
Access comprehensive regulatory information for “Techno-path” Multichem S Plus (Assayed) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 651d3c47ca2e397dcb1c50a31fc640ed 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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