Taiwan FDA registration a7c61d9f1d3c3a34c29e4553ee824a31
"Taylor Freis" Gibek Heat and Moisture Condenser (Artificial Nose) (Unsterilized)
TW: "泰勒弗瑞斯" 吉倍克熱及濕氣凝結器(人工鼻) (未滅菌)
Registration details
- Analysis ID
- a7c61d9f1d3c3a34c29e4553ee824a31
- Customs Code
- DHA04400962500
Company information
- Manufacturer
- TELEFLEX MEDICAL SDN BHD
- Manufacturer Country
- Malaysia
- Authorized Representative
- WESSON MEDICAL CO., LTD.
Product details
- Intended Use
- Limited to the first level recognition range of the Measures for the Administration of Medical Devices "Heat and Moisture Condenser (Artificial Nose) (D.5375)".
- Product Type (Level 1)
- D Anesthesiology
- Product Type (Level 2)
- D.5375 Heat and humidity condenser (artificial nose)
- Import Information
- import
Dates and status
- Registration Date
- Dec 08, 2010
- Expiry Date
- Dec 08, 2015
- Cancellation Date
- Jun 25, 2018
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Taylor Freis" Gibek Heat and Moisture Condenser (Artificial Nose) (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number a7c61d9f1d3c3a34c29e4553ee824a31 and manufactured by TELEFLEX MEDICAL SDN BHD. The authorized representative in Taiwan is WESSON MEDICAL CO., 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