"Siemens" fully automatic urine analyzer (unsterilized)
Taiwan·Risk Class 1·SPARTON MEDICAL SYSTEMS;; SIEMENS HEALTHCARE DIAGNOSTICS INC.·Registered Sep 21, 2010 – Sep 21, 2020Cancelled- Analysis ID
- a914ed4df675ee8338b6149bb048d8ca
- Customs Code
- DHA04400923105
- Manufacturer Country
- United States
- 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
- Sep 21, 2010
- Expiry Date
- Sep 21, 2020
- Cancellation Date
- May 19, 2022
- Status
- Logged out
- Reason
- 自行鍵入
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Access comprehensive regulatory information for "Siemens" fully automatic 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 a914ed4df675ee8338b6149bb048d8ca and manufactured by SPARTON MEDICAL SYSTEMS;; 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 77 Electronics Instrument Industry 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.