Taiwan FDA registration 720e8f22f756d452a03bb0c9bd81e710
"Urilyzer" Sed Control Set (Non-sterile)
TW: "康比"尿沉渣品管液(未滅菌)
Taiwan·Risk Class 1·MD·Analyticon Biotechnologies GmbH·Registered Sep 12, 2019 – Sep 12, 2024ExpiredRegistration details
- Analysis ID
- 720e8f22f756d452a03bb0c9bd81e710
- License Form
- Ministry of Health Medical Device Import No. 020857
- Customs Code
- DHA09402085707
Company information
- Manufacturer
- Analyticon Biotechnologies GmbH
- Manufacturer Country
- Germany
- Authorized Representative
- IN FUNG CO., LTD.
Product details
- Intended Use
- Limited to the first level identification range of quality control materials (analytical and non-analytical) (A.1660) of the Measures for the Administration of Medical Devices.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A1660 Quality Control Materials (Analytical and Non-Analytical)
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Sep 12, 2019
- Expiry Date
- Sep 12, 2024
About this record
Access comprehensive regulatory information for "Urilyzer" Sed Control Set (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 720e8f22f756d452a03bb0c9bd81e710 and manufactured by Analyticon Biotechnologies GmbH. The authorized representative in Taiwan is IN FUNG CO., LTD..
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