Taiwan FDA registration 4dd3649b8235b31766264a27443f009e
VITEK 2 Gram Positive AST for Teicoplanin
TW: 微鐵克2革蘭氏陽性菌藥敏卡抗生素-太古盤寧
Registration details
- Analysis ID
- 4dd3649b8235b31766264a27443f009e
- License Form
- Ministry of Health Medical Device Import No. 032474
- Customs Code
- DHA05603247400
Company information
- Manufacturer
- bioMérieux, Inc.
- Manufacturer Country
- United States
- Authorized Representative
- Hong Kong Commercial Mérieux S.p.A. Taiwan Branch
Product details
- Intended Use
- This product can be used with Microtek 2 automatic microbial analyzer to determine the antibiotic susceptibility of Staphylococcus, Enterococcus and Streptococcus agalactis to Teicoplanin in vitro in clinical laboratories.
- 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
- Aug 05, 2019
- Expiry Date
- Aug 05, 2024
About this record
Access comprehensive regulatory information for VITEK 2 Gram Positive AST for Teicoplanin in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 4dd3649b8235b31766264a27443f009e and manufactured by bioMérieux, Inc.. 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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