Taiwan FDA registration fe98d7cc5edb1dff18406921ed465221
Phadia System (Non-Sterile)
TW: 法迪亞(自動化儀器)系列(未滅菌)
Taiwan·Risk Class 1·MD·PHADIA AB·Registered Oct 01, 2021 – Oct 31, 2026ActiveRegistration details
- Analysis ID
- fe98d7cc5edb1dff18406921ed465221
- License Form
- Ministry of Health Medical Device Import Registration No. 005250
- Customs Code
- DHA08400525002
Company information
- Manufacturer
- PHADIA AB
- Manufacturer Country
- Sweden
- Authorized Representative
- PHADIA TAIWAN INC.
Product details
- Intended Use
- Limited to the first level identification range of the "Individual Photometric Chemical Analyzer for Clinical Use (A.2160)" of the Measures for the Administration of Medical Devices.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A2160 Individual photometric chemistry analyzer for clinical use
- 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 Phadia System (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 fe98d7cc5edb1dff18406921ed465221 and manufactured by PHADIA AB. The authorized representative in Taiwan is PHADIA TAIWAN INC..
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