"Miyasu Kimori" Fully automatic urine and fluid analyzer (unsterilized)
Taiwan·Risk Class 1·SYSMEX CORPORATION, I-SQUARE·Registered Mar 23, 2016 – Mar 23, 2026Cancelled- Analysis ID
- 8586f54d3dbec2a4ad71d012a3406d6e
- Customs Code
- DHA09401631100
- Manufacturer
- SYSMEX CORPORATION, I-SQUARE
- Manufacturer Country
- Japan
- Authorized Representative
- SYSMEX TAIWAN CO., LTD.
- 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
- Input;; QMS/QSD
- Registration Date
- Mar 23, 2016
- Expiry Date
- Mar 23, 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 "Miyasu Kimori" Fully automatic urine and fluid 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 8586f54d3dbec2a4ad71d012a3406d6e and manufactured by SYSMEX CORPORATION, I-SQUARE. The authorized representative in Taiwan is SYSMEX TAIWAN CO., LTD..
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including SYSMEX CORPORATION;; SYSMEX CORPORATION, I-SQUARE, 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.