Taiwan FDA registration 433da75e2747be66dd9e2f0070f711c1
Combi Screen XL (Non-Sterile)
TW: 康比自動尿液分析儀 (未滅菌)
Taiwan·Risk Class 1·MD·ANALYTICON BIOTECHNOLOGIES AG·Registered Oct 01, 2021 – Oct 31, 2023ExpiredRegistration details
- Analysis ID
- 433da75e2747be66dd9e2f0070f711c1
- License Form
- Ministry of Health Medical Device Import Registration No. 006381
- Customs Code
- DHA08400638106
Company information
- Manufacturer
- ANALYTICON BIOTECHNOLOGIES AG
- Manufacturer Country
- Germany
- Authorized Representative
- IN FUNG 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)
- A2900 Automated Urinalysis System
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Oct 01, 2021
- Expiry Date
- Oct 31, 2023
About this record
Access comprehensive regulatory information for Combi Screen XL (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 433da75e2747be66dd9e2f0070f711c1 and manufactured by ANALYTICON BIOTECHNOLOGIES AG. The authorized representative in Taiwan is IN FUNG CO., LTD..
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