Taiwan FDA registration 78226b4996ffd57359bf7fe5f4190da2
"Covidien" Airway connector (Non-Sterile)
TW: "柯迪恩" 氣道連接器 (未滅菌)
Taiwan·Risk Class 1·MD·COVIDIEN LLC·Registered Mar 05, 2018 – Mar 05, 2023ExpiredRegistration details
- Analysis ID
- 78226b4996ffd57359bf7fe5f4190da2
- License Form
- Ministry of Health Medical Device Import No. 018865
- Customs Code
- DHA09401886501
Company information
- Manufacturer
- COVIDIEN LLC
- Manufacturer Country
- United States
- Authorized Representative
- ELC ENTERPRISE LTD.
Product details
- Intended Use
- Limited to the first level identification range of the "Airway Connector (D.5810)" of the Measures for the Administration of Medical Devices.
- Product Type (Level 1)
- D Devices for anesthesiology
- Product Type (Level 2)
- D5810 airway connector
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Mar 05, 2018
- Expiry Date
- Mar 05, 2023
About this record
Access comprehensive regulatory information for "Covidien" Airway connector (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 78226b4996ffd57359bf7fe5f4190da2 and manufactured by COVIDIEN LLC. The authorized representative in Taiwan is ELC ENTERPRISE 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