Taiwan FDA registration db52719c139df09b741b11afc53e1e42
"Ciji" suction catheter (sterilized)
TW: “慈耆”抽吸導管 (滅菌)
Taiwan·Risk Class 1·SHANGHAI TSYRCHI TRADING CO., LTD·Registered Jul 22, 2008 – Jul 22, 2013CancelledRegistration details
- Analysis ID
- db52719c139df09b741b11afc53e1e42
- Customs Code
- DHA04600053904
Company information
- Manufacturer
- SHANGHAI TSYRCHI TRADING CO., LTD
- Manufacturer Country
- China
- Authorized Representative
- FAIRY POLYMER INDUSTRY CO., LTD.
Product details
- Intended Use
- Limited to the management method of medical equipment, tracheobronchial suction catheter (D.6810) level 1 identification range.
- Product Type (Level 1)
- D Anesthesiology
- Product Type (Level 2)
- D.6810 Pneumatic bronchial suction guide tube
- Import Information
- Input;; Chinese goods
Dates and status
- Registration Date
- Jul 22, 2008
- Expiry Date
- Jul 22, 2013
- Cancellation Date
- Jun 02, 2015
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Ciji" suction catheter (sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number db52719c139df09b741b11afc53e1e42 and manufactured by SHANGHAI TSYRCHI TRADING CO., LTD. The authorized representative in Taiwan is FAIRY POLYMER INDUSTRY 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