Taiwan FDA registration 30213f0ed0f2af652c35aa004761a3fb
"Enosan" percutaneous endoscopic gastrostomy group
TW: "愛諾生" 經皮內視鏡胃造瘻組
Taiwan·Risk Class 2·AVENT, INC.;; Avanos Medical, Inc.·Registered Jul 03, 2006 – Jul 03, 2026ExpiredRegistration details
- Analysis ID
- 30213f0ed0f2af652c35aa004761a3fb
- Customs Code
- DHA00601678101
Company information
- Manufacturer
- AVENT, INC.;; Avanos Medical, Inc.
- Manufacturer Country
- United States
- Authorized Representative
- CHINA HOSMED INTERNATIONAL INC.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- H Gastroenterology and urology
- Import Information
- Input;; Contract manufacturing
Dates and status
- Registration Date
- Jul 03, 2006
- Expiry Date
- Jul 03, 2026
About this record
Access comprehensive regulatory information for "Enosan" percutaneous endoscopic gastrostomy group in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 30213f0ed0f2af652c35aa004761a3fb and manufactured by AVENT, INC.;; Avanos Medical, Inc.. The authorized representative in Taiwan is CHINA HOSMED INTERNATIONAL INC..
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