"Abbott" Esther bedside blood monitor
Taiwan·Risk Class 2·ABBOTT POINT OF CARE INC.;; Abbott Point of Care Inc.·Registered Mar 14, 2019 – Mar 14, 2029Active- Analysis ID
- 40053c28cd029e1b673adc06328ba24d
- Customs Code
- DHA05603237307
- Manufacturer Country
- United States
- Authorized Representative
- ABBOTT LABORATORIES SERVICES LLC TAIWAN BRANCH (U.S.A.)
- Intended Use
- Change the performance (adjust the text description) to: This product needs to be equipped with an i-STAT chip cassette, which is used to quantitatively detect various analytes in arterial, venous and microvascular whole blood.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1345 Glucose Test System;; A.1145 Calcium testing system;; A.1770 Urea nitrogen test system
- Import Information
- Contract manufacturing;; input
- Registration Date
- Mar 14, 2019
- Expiry Date
- Mar 14, 2029
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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 40053c28cd029e1b673adc06328ba24d and manufactured by ABBOTT POINT OF CARE INC.;; Abbott Point of Care Inc.. 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.;; FLEXTRONICS MANUFACTURING (SINGAPORE) PTE LTD, 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.