Taiwan FDA registration 39160a71b349b94e5bbc74620dd5550c
AQUALAB Urinalysis Tester PU-4010 (Unsterilized)
TW: “愛科來”尿液分析檢測儀 PU-4010(未滅菌)
Taiwan·Risk Class 1·ARKRAY FACTORY INC.·Registered Apr 26, 2010 – Apr 26, 2025CancelledRegistration details
- Analysis ID
- 39160a71b349b94e5bbc74620dd5550c
- Customs Code
- DHA04400877106
Company information
- Manufacturer
- ARKRAY FACTORY INC.
- Manufacturer Country
- Japan
- Authorized Representative
- MEDTRI CO., LTD.
Product details
- 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
Dates and status
- Registration Date
- Apr 26, 2010
- Expiry Date
- Apr 26, 2025
- Cancellation Date
- Sep 30, 2021
Cancellation information
- Status
- Logged out
- Reason
- 轉為登錄字號
About this record
Access comprehensive regulatory information for AQUALAB Urinalysis Tester PU-4010 (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 39160a71b349b94e5bbc74620dd5550c and manufactured by ARKRAY FACTORY INC.. The authorized representative in Taiwan is MEDTRI CO., LTD..
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