Taiwan FDA registration 1760bb2d3160a79bee12e87b7de6578d
Abbott Designer Plus Analyzer
TW: 亞培設計師Plus分析儀
Taiwan·Risk Class 1·ABBOTT LABORATORIES·Registered Jun 07, 2010 – Jun 07, 2015CancelledRegistration details
- Analysis ID
- 1760bb2d3160a79bee12e87b7de6578d
- Customs Code
- DHA04400888001
Company information
- Manufacturer
- ABBOTT LABORATORIES
- Manufacturer Country
- United States
- Authorized Representative
- ABBOTT LABORATORIES SERVICES LLC TAIWAN BRANCH (U.S.A.)
Product details
- Intended Use
- Limited to the first level identification range of enzyme analyzer for clinical use (A.2500) of the Measures for the Administration of Medical Devices.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.2500 Enzyme analyzer for clinical use
- Import Information
- import
Dates and status
- Registration Date
- Jun 07, 2010
- Expiry Date
- Jun 07, 2015
- Cancellation Date
- Aug 09, 2018
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for Abbott Designer Plus Analyzer in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 1760bb2d3160a79bee12e87b7de6578d and manufactured by ABBOTT LABORATORIES. The authorized representative in Taiwan is ABBOTT LABORATORIES SERVICES LLC TAIWAN BRANCH (U.S.A.).
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