Taiwan FDA registration 9850e40b710a3bcdec9ab344ea10b168
"Medite" suction regulator (unsterilized)
TW: “美德特”吸引調節器 (未滅菌)
Registration details
- Analysis ID
- 9850e40b710a3bcdec9ab344ea10b168
- Customs Code
- DHY04300266601
Company information
- Manufacturer
- TUNGSHI MEDICAL EQUIPMENT CO., LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- YI LIN ENTERPRISE CO., LTD.
Product details
- Intended Use
- Limited to the first level recognition range of the classification and grading management measures for medical equipment "Vacuum-powered body fluid absorption device (J.6740)".
- Product Type (Level 1)
- J General hospital and personal use equipment
- Product Type (Level 2)
- J.6740 Vacuum-powered fluid absorption apparatus
- Import Information
- 委託製造;; 國產;; QMS/QSD
Dates and status
- Registration Date
- Oct 22, 2009
- Expiry Date
- Oct 22, 2024
About this record
Access comprehensive regulatory information for "Medite" suction regulator (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 9850e40b710a3bcdec9ab344ea10b168 and manufactured by TUNGSHI MEDICAL EQUIPMENT CO., LTD.. The authorized representative in Taiwan is YI LIN ENTERPRISE 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