Taiwan FDA registration 79762346149f59dca950d16ff2ebacd7
"Copper seal" suction regulator (unsterilized)
TW: "銅璽"吸引調節器 (未滅菌)
Registration details
- Analysis ID
- 79762346149f59dca950d16ff2ebacd7
Company information
- Manufacturer
- TUNGSHI MEDICAL EQUIPMENT CO., LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- TUNGSHI MEDICAL EQUIPMENT CO., LTD.
Product details
- Intended Use
- Limited to the first level recognition range of the Measures for the Administration of Medical Devices "Vacuum-powered Body Fluid Absorption Devices (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
- QMS/QSD;; 國產
Dates and status
- Registration Date
- Sep 17, 2013
- Expiry Date
- Sep 17, 2023
- Cancellation Date
- Mar 29, 2024
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Copper seal" 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 79762346149f59dca950d16ff2ebacd7 and manufactured by TUNGSHI MEDICAL EQUIPMENT CO., LTD.. The authorized representative in Taiwan is TUNGSHI MEDICAL EQUIPMENT 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