Taiwan FDA registration d431d21a67e488a74bcab39a2ed74fcb
BD Phoenix M50
TW: BD全自動微生物鑑定及藥敏性試驗分析儀
Taiwan·Risk Class 2·MD·BECTON, DICKINSON AND COMPANY·Registered Jan 26, 2017 – Jan 26, 2027ActiveRegistration details
- Analysis ID
- d431d21a67e488a74bcab39a2ed74fcb
- License Form
- Ministry of Health Medical Device Import No. 029313
- Customs Code
- DHA05602931305
Company information
- Manufacturer
- BECTON, DICKINSON AND COMPANY
- Manufacturer Country
- United States
- Authorized Representative
- BECTON DICKINSON HOLDINGS PTE. LTD. TAIWAN BRANCH (SINGAPORE)
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order.
- Product Type (Level 1)
- C Immunology and microbiology devices
- Product Type (Level 2)
- C1645 Automatic Short Incubation Period Antibiotic Susceptibility Testing System
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jan 26, 2017
- Expiry Date
- Jan 26, 2027
About this record
Access comprehensive regulatory information for BD Phoenix M50 in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d431d21a67e488a74bcab39a2ed74fcb and manufactured by BECTON, DICKINSON AND COMPANY. The authorized representative in Taiwan is BECTON DICKINSON HOLDINGS PTE. LTD. TAIWAN BRANCH (SINGAPORE).
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.
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