Taiwan FDA registration 8d94717f9dae15305e256cb8b2f5cd4d
"Barditek" Ekoma Immunofluorescence Analyzer (Unsterilized)
TW: "巴迪鐵克" 艾闊瑪免疫螢光分析儀 (未滅菌)
Taiwan·Risk Class 1·Boditech Med Inc.·Registered May 24, 2023 – Oct 31, 2025ExpiredRegistration details
- Analysis ID
- 8d94717f9dae15305e256cb8b2f5cd4d
- Customs Code
- DHA084a0018101
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
- May 24, 2023
- Expiry Date
- Oct 31, 2025
About this record
Access comprehensive regulatory information for "Barditek" Ekoma 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 8d94717f9dae15305e256cb8b2f5cd4d and manufactured by Boditech Med Inc.. The authorized representative in Taiwan is MEDRICH INSTRUMENT CO., LTD..
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.
Free DatabasePowered by Pure Global AI89,000+ Devices