"Siemens" 1800 biochemical analyzer (unsterilized)
Taiwan·Risk Class 1·JEOL LTD.;; SIEMENS HEALTHCARE DIAGNOSTICS INC.·Registered Aug 21, 2008 – Aug 21, 2023Cancelled- Analysis ID
- 49308144ecd248bed15eae96fe9db929
- Customs Code
- DHA04400701005
- Manufacturer
- JEOL LTD.;; SIEMENS HEALTHCARE DIAGNOSTICS INC.
- Manufacturer Country
- United States;;Japan
- Authorized Representative
- SIEMENS HEALTHCARE LIMITED
- Intended Use
- Limited to the first level identification range of the "Individual Photometric Chemical Analyzer for Clinical Use (A.2160)" of the Measures for the Administration of Medical Devices. Usage Dosage =
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.2160 Individual Photometric Chemistry Analyzer for Clinical Use
- Import Information
- import
- Registration Date
- Aug 21, 2008
- Expiry Date
- Aug 21, 2023
- 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" 1800 biochemical 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 49308144ecd248bed15eae96fe9db929 and manufactured by JEOL LTD.;; 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 JEOL LTD.;; 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.