Taiwan FDA registration 236d62ed4755c19d938583b6c924dee4
Teleflex tubing fixture (sterilization)
TW: “泰利福”氣管管路固定裝置 (滅菌)
Taiwan·Risk Class 1·Teleflex Medical Sdn.Bhd.·Registered Jun 24, 2013 – Jun 24, 2018CancelledRegistration details
- Analysis ID
- 236d62ed4755c19d938583b6c924dee4
- Customs Code
- DHA04401313600
Company information
- Manufacturer
- Teleflex Medical Sdn.Bhd.
- Manufacturer Country
- Malaysia
- Authorized Representative
- TELEFLEX MEDICAL TAIWAN LTD.
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
- QMS/QSD;; 輸入
Dates and status
- Registration Date
- Jun 24, 2013
- Expiry Date
- Jun 24, 2018
- Cancellation Date
- Dec 20, 2019
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for Teleflex tubing fixture (sterilization) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 236d62ed4755c19d938583b6c924dee4 and manufactured by Teleflex Medical Sdn.Bhd.. The authorized representative in Taiwan is TELEFLEX MEDICAL TAIWAN 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