Taiwan FDA registration 10d61f9824a132063213d0ed090c1af0
Analyticon combi scan 500 (Non-Sterile)
TW: 康比尿液生化檢測試紙判讀機 (未滅菌)
Taiwan·Risk Class 1·MD·ANALYTICON BIOTECHNOLOGIES AG·Registered Oct 01, 2021 – Oct 31, 2026ActiveRegistration details
- Analysis ID
- 10d61f9824a132063213d0ed090c1af0
- License Form
- Ministry of Health Medical Device Import Registration No. 002271
- Customs Code
- DHA08400227105
Company information
- Manufacturer
- ANALYTICON BIOTECHNOLOGIES AG
- Manufacturer Country
- Germany
- Authorized Representative
- IN FUNG CO., LTD.
Product details
- Intended Use
- Automatic interpretation of urine test strips
- 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, 2026
About this record
Access comprehensive regulatory information for Analyticon combi scan 500 (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 10d61f9824a132063213d0ed090c1af0 and manufactured by ANALYTICON BIOTECHNOLOGIES AG. The authorized representative in Taiwan is IN FUNG CO., LTD..
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices