Ekenvirasti Urinalysis System (Unsterilized)
Taiwan·Risk Class 1·IRIS DIAGNOSTICS·Registered May 28, 2008 – May 28, 2018Cancelled- Analysis ID
- 247bfd3540508c4298fc4a236927f3e7
- Customs Code
- DHA04400676807
- Manufacturer
- IRIS DIAGNOSTICS
- Manufacturer Country
- United States
- Authorized Representative
- BECKMAN COULTER TAIWAN INC., TAIWAN BRANCH (U.S.A.)
- 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
- import
- Registration Date
- May 28, 2008
- Expiry Date
- May 28, 2018
- Cancellation Date
- Dec 13, 2019
- Status
- Logged out
- Reason
- 許可證已逾有效期
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Access comprehensive regulatory information for Ekenvirasti Urinalysis System (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 247bfd3540508c4298fc4a236927f3e7 and manufactured by IRIS DIAGNOSTICS. The authorized representative in Taiwan is BECKMAN COULTER TAIWAN INC., TAIWAN BRANCH (U.S.A.).
This page provides complete technical specifications, regulatory compliance details, 2 companies making similar products including BECKMAN COULTER, INC., IRIS DIAGNOSTICS, A DIVISION OF IRIS INTERNATIONAL, INC., and 4 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.