Taiwan FDA registration 0b8e9e0c8ecdc1b4c0178df4ee301ebe
“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 Apr 02, 2019 – Apr 02, 2024CancelledRegistration details
- Analysis ID
- 0b8e9e0c8ecdc1b4c0178df4ee301ebe
- License Form
- Ministry of Health Medical Device Import No. 032393
- Customs Code
- DHA05603239300
Company information
- Manufacturer
- TECHNO-PATH MANUFACTURING LTD
- Manufacturer Country
- Ireland
- Authorized Representative
- ABBOTT LABORATORIES SERVICES LLC TAIWAN BRANCH (U.S.A.)
Product details
- 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
- Apr 02, 2019
- Expiry Date
- Apr 02, 2024
- Cancellation Date
- Apr 22, 2022
Cancellation information
- Status
- Logged out
- Reason
- 自請註銷
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 0b8e9e0c8ecdc1b4c0178df4ee301ebe 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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