Taiwan FDA registration f63f6ddd16986bed7bffb18311c400fa
"Dirui" urine analyzer (unsterilized)
TW: "迪瑞" 尿液分析儀 (未滅菌)
Taiwan·Risk Class 1·DIRUI INDUSTRIAL CO., LTD.·Registered Jul 20, 2015 – Jul 20, 2020CancelledRegistration details
- Analysis ID
- f63f6ddd16986bed7bffb18311c400fa
- Customs Code
- DHA09600245402
Company information
- Manufacturer
- DIRUI INDUSTRIAL CO., LTD.
- Manufacturer Country
- China
- Authorized Representative
- TENG SIH ENTERPRISE COMPANY LIMITED
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
- QMS/QSD;; Input;; Chinese goods
Dates and status
- Registration Date
- Jul 20, 2015
- Expiry Date
- Jul 20, 2020
- Cancellation Date
- Jun 22, 2022
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Dirui" urine 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 f63f6ddd16986bed7bffb18311c400fa and manufactured by DIRUI INDUSTRIAL CO., LTD.. The authorized representative in Taiwan is TENG SIH ENTERPRISE COMPANY LIMITED.
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