"Abbott" Esther bedside blood monitor
Taiwan·Risk Class 2·ABBOTT POINT OF CARE INC.;; FLEXTRONICS MANUFACTURING (SINGAPORE) PTE LTD·Registered Nov 05, 2015 – Nov 05, 2025Expired- Analysis ID
- c24e22f95af58ec35686ad35f6664500
- Customs Code
- DHA05602790201
- Manufacturer Country
- United States;;Singapore
- Authorized Representative
- ABBOTT LABORATORIES SERVICES LLC TAIWAN BRANCH (U.S.A.)
- Intended Use
- Equipped with Abbott special chip cassette, the components in whole blood samples are quantitatively measured.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1120 血內氣體(PCO2,PO2)及血液pH值試驗系統
- Import Information
- Input;; Contract manufacturing
- Registration Date
- Nov 05, 2015
- Expiry Date
- Nov 05, 2025
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Access comprehensive regulatory information for "Abbott" Esther bedside blood monitor in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number c24e22f95af58ec35686ad35f6664500 and manufactured by ABBOTT POINT OF CARE INC.;; FLEXTRONICS MANUFACTURING (SINGAPORE) PTE 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, 1 companies making similar products including ABBOTT POINT OF CARE INC.;; Abbott Point of Care Inc., and 1 recent registrations in the same category. 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.