Taiwan FDA registration eafa3521c167a1b469e1fb74b2b84ea5
“Techno-path”Multichem S Plus (Unassayed)
TW: “泰可諾”多項目生化分析血清品管液(未分析)
Taiwan·Risk Class 2·MD·TECHNO-PATH MANUFACTURING LTD·Registered Apr 01, 2019 – Apr 01, 2024CancelledRegistration details
- Analysis ID
- eafa3521c167a1b469e1fb74b2b84ea5
- License Form
- Ministry of Health Medical Device Import No. 032392
- Customs Code
- DHA05603239201
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 01, 2019
- Expiry Date
- Apr 01, 2024
- Cancellation Date
- Sep 28, 2022
Cancellation information
- Status
- Logged out
- Reason
- 自請註銷
About this record
Access comprehensive regulatory information for “Techno-path”Multichem S Plus (Unassayed) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number eafa3521c167a1b469e1fb74b2b84ea5 and manufactured by TECHNO-PATH MANUFACTURING LTD. The authorized representative in Taiwan is ABBOTT LABORATORIES SERVICES LLC TAIWAN BRANCH (U.S.A.).
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices