"Siemens" desktop urine analyzer (unsterilized)
Taiwan·Risk Class 1·KIMBALL ELECTRONICS POLAND SP. ZO. O;; SIEMENS HEALTHCARE DIAGNOSTICS INC.·Registered Oct 01, 2021 – Oct 31, 2026Active- Analysis ID
- 03f27743193af907309c12293e9c6c76
- Customs Code
- DHA08400978506
- Manufacturer Country
- United States;;Poland
- Authorized Representative
- SIEMENS HEALTHCARE LIMITED
- Intended Use
- Limited to the first level identification range of the "Automated Urinalysis System (A.2900)" of the Measures for the Classification and Grading of Medical Devices.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.2900 Automated urinalysis system
- Import Information
- Contract manufacturing;; input
- Registration Date
- Oct 01, 2021
- Expiry Date
- Oct 31, 2026
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Access comprehensive regulatory information for "Siemens" desktop urine analyzer (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 03f27743193af907309c12293e9c6c76 and manufactured by KIMBALL ELECTRONICS POLAND SP. ZO. O;; SIEMENS HEALTHCARE DIAGNOSTICS INC.. The authorized representative in Taiwan is SIEMENS HEALTHCARE LIMITED.
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including KIMBALL ELECTRONICS POLAND SP. ZO. O;; SIEMENS HEALTHCARE DIAGNOSTICS 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.