"ARKRA" urinalysis tester (unsterilized)
Taiwan·Risk Class 1·Arkray Factory Inc., Head office factory·Registered Nov 17, 2006 – Nov 17, 2026Cancelled- Analysis ID
- 951471b6bf0cb1c7ac6052c4f09cbdda
- Customs Code
- DHA04400535401
- Manufacturer
- Arkray Factory Inc., Head office factory
- Manufacturer Country
- Japan
- Authorized Representative
- SYNGEN BIOTECH 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
- Registration Date
- Nov 17, 2006
- Expiry Date
- Nov 17, 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 "ARKRA" urinalysis tester (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 951471b6bf0cb1c7ac6052c4f09cbdda and manufactured by Arkray Factory Inc., Head office factory. The authorized representative in Taiwan is SYNGEN BIOTECH CO., LTD..
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including ARKRAY INDUSTRY, INC., and 2 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.