Taiwan FDA registration 851f8e6f067bab4a22b883ff946e75b9
"Large and medium" enema sleeve (unsterilized)
TW: “大中” 灌腸組套 (未滅菌)
Registration details
- Analysis ID
- 851f8e6f067bab4a22b883ff946e75b9
Company information
- Manufacturer
- DA CHUNG MEDICAL CO., LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- DA CHUNG MEDICAL CO., LTD.
Product details
- Intended Use
- Limited to the first level identification range of the "Enema Set (H.5210)" of the Measures for the Administration of Medical Equipment.
- Product Type (Level 1)
- H Gastroenterology and urology
- Product Type (Level 2)
- H.5210 手動式灌腸組套
- Import Information
- Domestic
Dates and status
- Registration Date
- Apr 16, 2014
- Expiry Date
- Apr 16, 2019
- Cancellation Date
- Jan 20, 2017
Cancellation information
- Status
- Logged out
- Reason
- 自請註銷
About this record
Access comprehensive regulatory information for "Large and medium" enema sleeve (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 851f8e6f067bab4a22b883ff946e75b9 and manufactured by DA CHUNG MEDICAL CO., LTD.. The authorized representative in Taiwan is DA CHUNG MEDICAL CO., LTD..
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.
Free DatabasePowered by Pure Global AI89,000+ Devices