Taiwan FDA registration fde595a232828a82f7b7a698b8b40a84
"Enoxen" Rapid Urease Test Reagent (Unsterilized)
TW: "愛諾生" 快速尿素酶檢驗試劑 (未滅菌)
Taiwan·Risk Class 1·AVENT, INC.;; Avanos Medical, Inc.·Registered Jul 25, 2005 – Jul 25, 2025ExpiredRegistration details
- Analysis ID
- fde595a232828a82f7b7a698b8b40a84
- Customs Code
- DHA04400026302
Company information
- Manufacturer
- AVENT, INC.;; Avanos Medical, Inc.
- Manufacturer Country
- United States
- Authorized Representative
- CHINA HOSMED INTERNATIONAL INC.
Product details
- Intended Use
- Determination of urease of pylori in gastric mucosal biopsy.
- Product Type (Level 1)
- C Immunology and microbiology
- Import Information
- Input;; Contract manufacturing
Dates and status
- Registration Date
- Jul 25, 2005
- Expiry Date
- Jul 25, 2025
About this record
Access comprehensive regulatory information for "Enoxen" Rapid Urease Test Reagent (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number fde595a232828a82f7b7a698b8b40a84 and manufactured by AVENT, INC.;; Avanos Medical, Inc.. The authorized representative in Taiwan is CHINA HOSMED INTERNATIONAL INC..
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