Taiwan FDA registration 748ef173b061c72464706d945e522daf
"Badiec" Efia immunofluorescence analyzer (unsterilized)
TW: "巴迪鐵克" 艾菲雅仕免疫螢光分析儀 (未滅菌)
Taiwan·Risk Class 1·Boditech Med Inc.·Registered Aug 29, 2023 – Oct 31, 2025ExpiredRegistration details
- Analysis ID
- 748ef173b061c72464706d945e522daf
- Customs Code
- DHA084a0021709
Company information
- Manufacturer
- Boditech Med Inc.
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- MEDRICH 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
- Aug 29, 2023
- Expiry Date
- Oct 31, 2025
About this record
Access comprehensive regulatory information for "Badiec" Efia immunofluorescence analyzer (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 748ef173b061c72464706d945e522daf and manufactured by Boditech Med Inc.. The authorized representative in Taiwan is MEDRICH INSTRUMENT CO., LTD..
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