"FUJI" DRI-CHEM IMMUNO AG1 (Non-Sterile)
Taiwan·Risk Class 1·MD·TERASAKI ELECTRIC CO., LTD. SYSTEM DIV. YAO FACTORY·Registered Oct 01, 2021 – Oct 31, 2023Expired- Analysis ID
- 2846d3b725bb90ea715adb2666ce3417
- License Form
- Ministry of Health Medical Device Import Registration No. 018792
- Customs Code
- DHA08401879204
- Manufacturer Country
- Japan
- Authorized Representative
- HUNG CHONG CORP.
- Intended Use
- Limited to the first level identification range of "Colorimeter, Photometer or Spectrophotometer for Clinical Use (A.2300)" under the Measures for the Administration of Medical Devices.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A2300 Colorimeter, photometer, or spectrophotometer for clinical use
- Import Information
- Imported from abroad
- Registration Date
- Oct 01, 2021
- Expiry Date
- Oct 31, 2023
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Access comprehensive regulatory information for "FUJI" DRI-CHEM IMMUNO AG1 (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 2846d3b725bb90ea715adb2666ce3417 and manufactured by TERASAKI ELECTRIC CO., LTD. SYSTEM DIV. YAO FACTORY. The authorized representative in Taiwan is HUNG CHONG CORP..
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