Taiwan FDA registration 485c00f22794ff9f169b6182b6c3ab4e
"Trifis " Pro-Evock chest drainage system
TW: “ 特立菲斯 ”普羅-愛渥克胸腔引流系統
Taiwan·Risk Class 1·TELEFLEX MEDICAL·Registered Apr 28, 2006 – Apr 28, 2011CancelledRegistration details
- Analysis ID
- 485c00f22794ff9f169b6182b6c3ab4e
- Customs Code
- DHA04400426803
Company information
- Manufacturer
- TELEFLEX MEDICAL
- Manufacturer Country
- United States
- Authorized Representative
- HSIN TUNG MEDICAL CO., LTD.
Product details
- Intended Use
- It is limited to the scope of the first level of identification of the "Vacuum-powered Body Fluid Absorption Appliances (J.6740)" of the Administrative Measures for Medical Devices.
- Product Type (Level 1)
- J General hospital and personal use equipment
- Product Type (Level 2)
- J.6740 Vacuum-powered fluid absorption apparatus
- Import Information
- import
Dates and status
- Registration Date
- Apr 28, 2006
- Expiry Date
- Apr 28, 2011
- Cancellation Date
- May 06, 2011
Cancellation information
- Status
- Logged out
- Reason
- 自請註銷
About this record
Access comprehensive regulatory information for "Trifis " Pro-Evock chest drainage system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 485c00f22794ff9f169b6182b6c3ab4e and manufactured by TELEFLEX MEDICAL. The authorized representative in Taiwan is HSIN TUNG 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