Taiwan FDA registration 365ac7895d50e2161d6c97ae8c9f6147
"Active" endotracheal tube fixation belt (unsterilized)
TW: "活絡"氣管內管固定帶 (未滅菌)
Taiwan·Risk Class 1·FERNO-WASHINGTON, INC.·Registered Apr 13, 2006 – Apr 13, 2011CancelledRegistration details
- Analysis ID
- 365ac7895d50e2161d6c97ae8c9f6147
- Customs Code
- DHA04400380103
Company information
- Manufacturer
- FERNO-WASHINGTON, INC.
- Manufacturer Country
- United States
- Authorized Representative
- TARGETLINE INCORPORATED
Product details
- Intended Use
- Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Tracheal Pipeline Fixation Device (D.5770)".
- Product Type (Level 1)
- D Anesthesiology
- Product Type (Level 2)
- D.5770 氣管管路固定裝置
- Import Information
- import
Dates and status
- Registration Date
- Apr 13, 2006
- Expiry Date
- Apr 13, 2011
- Cancellation Date
- Oct 29, 2012
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Active" endotracheal tube fixation belt (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 365ac7895d50e2161d6c97ae8c9f6147 and manufactured by FERNO-WASHINGTON, INC.. The authorized representative in Taiwan is TARGETLINE INCORPORATED.
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