Taiwan FDA registration d0d6c5ec80c1b435f30c5f2fa1dcbf4d
Crystallized fluorescence instrument for clinical use (unsterilized)
TW: 晶實 臨床使用的螢光儀 (未滅菌)
Taiwan·Risk Class 1·DiagnOptics Technologies B.V.·Registered May 17, 2023 – Oct 31, 2025ExpiredRegistration details
- Analysis ID
- d0d6c5ec80c1b435f30c5f2fa1dcbf4d
- Customs Code
- DHA084a0017901
Company information
- Manufacturer
- DiagnOptics Technologies B.V.
- Manufacturer Country
- Netherlands
- Authorized Representative
- JINGS INSTRUMENT CO., LTD.
Product details
- Intended Use
- Limited to the classification and grading management measures of medical equipment "fluorescence instrument for clinical use (A.2560)" the first level identification range.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.2560 Fluorometer for clinical use
Dates and status
- Registration Date
- May 17, 2023
- Expiry Date
- Oct 31, 2025
About this record
Access comprehensive regulatory information for Crystallized fluorescence instrument for clinical use (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number d0d6c5ec80c1b435f30c5f2fa1dcbf4d and manufactured by DiagnOptics Technologies B.V.. The authorized representative in Taiwan is JINGS INSTRUMENT CO., LTD..
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