Taiwan FDA registration ac4d50ae5db45c1f1a43ff4411bc2efa
Diry urine analyzer
TW: 迪瑞尿液分析儀
Taiwan·Risk Class 1·DIRUI INDUSTRIAL CO., LTD.·Registered Aug 08, 2008 – Aug 08, 2013CancelledRegistration details
- Analysis ID
- ac4d50ae5db45c1f1a43ff4411bc2efa
- Customs Code
- DHA04600055808
Company information
- Manufacturer
- DIRUI INDUSTRIAL CO., LTD.
- Manufacturer Country
- China
- Authorized Representative
- TENG SIH ENTERPRISE COMPANY LIMITED
Product details
- Intended Use
- It is limited to the scope of the first level of identification of the "Automatic Urinalysis System (A.2900)" of the Administrative Measures for Medical Devices. Dosage =
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.2900 Automated urinalysis system
- Import Information
- Chinese goods;; input
Dates and status
- Registration Date
- Aug 08, 2008
- Expiry Date
- Aug 08, 2013
- Cancellation Date
- Aug 28, 2015
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for Diry urine analyzer in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number ac4d50ae5db45c1f1a43ff4411bc2efa and manufactured by DIRUI INDUSTRIAL CO., LTD.. The authorized representative in Taiwan is TENG SIH ENTERPRISE COMPANY LIMITED.
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