Taiwan FDA registration e39aaf0dcf9ffc2e3046e5954b201032
Sensititre YeastOne Broth
TW: 先瑟特爾真菌藥敏測試培養液
Taiwan·Risk Class 2·MD·REMEL INC.·Registered Oct 03, 2019 – Oct 03, 2024ExpiredRegistration details
- Analysis ID
- e39aaf0dcf9ffc2e3046e5954b201032
- License Form
- Ministry of Health Medical Device Import No. 032933
- Customs Code
- DHA05603293306
Company information
- Manufacturer
- REMEL INC.
- Manufacturer Country
- United States
- Authorized Representative
- THERMO FISHER SCIENTIFIC TAIWAN CO., LTD.
Product details
- Intended Use
- This product is an in vitro diagnostic product tested for potency testing with the Sensititre System for non-picky yeasts, including Candida spp. , Cryptococcus spp. Aspergillus spp. and the cultivation of various other fast-growing yeast species.
- Product Type (Level 1)
- C Immunology and microbiology devices
- Product Type (Level 2)
- C1700 Antimicrobial susceptibility test medium
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Oct 03, 2019
- Expiry Date
- Oct 03, 2024
About this record
Access comprehensive regulatory information for Sensititre YeastOne Broth in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e39aaf0dcf9ffc2e3046e5954b201032 and manufactured by REMEL INC.. The authorized representative in Taiwan is THERMO FISHER SCIENTIFIC TAIWAN CO., LTD..
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