Taiwan FDA registration 40958fa8901a28c19047e224f053b180
ATB PSE CLSI (12)
TW: 優必非發酵菌藥物敏感性試驗套組
Taiwan·Risk Class 2·MD·bioMérieux SA·Registered Dec 28, 2017 – Dec 28, 2022ExpiredRegistration details
- Analysis ID
- 40958fa8901a28c19047e224f053b180
- License Form
- Ministry of Health Medical Device Import No. 030476
- Customs Code
- DHA05603047607
Company information
- Manufacturer
- bioMérieux SA
- Manufacturer Country
- France
- Authorized Representative
- Hong Kong Commercial Mérieux S.p.A. Taiwan Branch
Product details
- Intended Use
- This product is used for drug susceptibility test of Pseudomona and other non-fermented gram-negative bacilli.
- Product Type (Level 1)
- C Immunology and microbiology devices
- Product Type (Level 2)
- C1640 Antimicrobial susceptibility test powder
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Dec 28, 2017
- Expiry Date
- Dec 28, 2022
About this record
Access comprehensive regulatory information for ATB PSE CLSI (12) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 40958fa8901a28c19047e224f053b180 and manufactured by bioMérieux SA. The authorized representative in Taiwan is Hong Kong Commercial Mérieux S.p.A. Taiwan Branch.
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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