Taiwan FDA registration 67e722e95a0134a38ad63c3ec04f9600
Teleflex airway connector (unsterilized)
TW: "泰利福" 氣道連接器 (未滅菌)
Taiwan·Risk Class 1·TELEFLEX MEDICAL·Registered May 24, 2011 – May 24, 2021CancelledRegistration details
- Analysis ID
- 67e722e95a0134a38ad63c3ec04f9600
- Customs Code
- DHA04401039407
Company information
- Manufacturer
- TELEFLEX MEDICAL
- Manufacturer Country
- Mexico
- Authorized Representative
- BENQ MEDICAL TECHNOLOGY CORPORATION
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 Anesthesiology
- Product Type (Level 2)
- D.5810 Airway connectors
- Import Information
- import
Dates and status
- Registration Date
- May 24, 2011
- Expiry Date
- May 24, 2021
- Cancellation Date
- Nov 08, 2018
Cancellation information
- Status
- Logged out
- Reason
- 自請註銷
About this record
Access comprehensive regulatory information for Teleflex airway connector (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 67e722e95a0134a38ad63c3ec04f9600 and manufactured by TELEFLEX MEDICAL. The authorized representative in Taiwan is BENQ MEDICAL TECHNOLOGY CORPORATION.
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