Taiwan FDA registration ad9c3d58c6f45e0e27d8151639f1c669
"Teleflex" Nasal oxygen cannula (non-sterile)
TW: "泰樂福"經鼻氧氣套管 (未滅菌)
Taiwan·Risk Class 1·MD·Teleflex Medical·Registered Oct 03, 2017 – Oct 03, 2022CancelledRegistration details
- Analysis ID
- ad9c3d58c6f45e0e27d8151639f1c669
- License Form
- Ministry of Health Medical Device Import No. 018381
- Customs Code
- DHA09401838105
Company information
- Manufacturer
- Teleflex Medical
- Manufacturer Country
- United States
- Authorized Representative
- AIR LIQUIDE FAR EASTERN LTD.
Product details
- Product Type (Level 1)
- D Devices for anesthesiology
- Product Type (Level 2)
- D5340 Transnasal oxygen cannula
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Oct 03, 2017
- Expiry Date
- Oct 03, 2022
- Cancellation Date
- Oct 11, 2022
Cancellation information
- Status
- Logged out
- Reason
- 自請註銷
About this record
Access comprehensive regulatory information for "Teleflex" Nasal oxygen cannula (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 ad9c3d58c6f45e0e27d8151639f1c669 and manufactured by Teleflex Medical. The authorized representative in Taiwan is AIR LIQUIDE FAR EASTERN 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