"Siemens" desktop urine analyzer (unsterilized)
Taiwan·Risk Class 1·KIMBALL ELECTRONICS POLAND SP. ZO. O;; SIEMENS HEALTHCARE DIAGNOSTICS INC.·Registered Jan 10, 2011 – Jan 10, 2026Cancelled- Analysis ID
- 00a5b1e0f3a4ce72d7a31a6f46af50ea
- Customs Code
- DHA04400978509
- Manufacturer Country
- United States;;Poland
- Authorized Representative
- SIEMENS HEALTHCARE LIMITED
- Intended Use
- Limited to the first level identification range of the "Automatic Urinalysis System (A.2900)" of the Measures for the Administration 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
- Jan 10, 2011
- Expiry Date
- Jan 10, 2026
- Cancellation Date
- Sep 30, 2021
- Status
- Logged out
- Reason
- 轉為登錄字號
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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 00a5b1e0f3a4ce72d7a31a6f46af50ea 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.