Taiwan FDA registration b5230e50216b7f656999cf5248662454
Fadia Automation Instrument Series (Non-Sterile)
TW: 法迪亞 自動化儀器系列 (未滅菌)
Taiwan·Risk Class 1·PHADIA AB·Registered Dec 24, 2024 – Oct 31, 2026ActiveRegistration details
- Analysis ID
- b5230e50216b7f656999cf5248662454
- Customs Code
- DHA084A0034202
Company information
- Manufacturer
- PHADIA AB
- Manufacturer Country
- Sweden
- Authorized Representative
- PHADIA TAIWAN INC.
Product details
- Intended Use
- It is limited to the first level of identification of the classification and grading management of medical devices "Individual Photometric Chemical Analyzer for Clinical Use (A.2160)".
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.2160 Individual Photometric Chemistry Analyzer for Clinical Use
- Import Information
- import
Dates and status
- Registration Date
- Dec 24, 2024
- Expiry Date
- Oct 31, 2026
About this record
Access comprehensive regulatory information for Fadia Automation Instrument Series (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 b5230e50216b7f656999cf5248662454 and manufactured by PHADIA AB. The authorized representative in Taiwan is PHADIA TAIWAN INC..
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.
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