Taiwan FDA registration ff2b8e9ec2bb05598cc0f3fc65d72aae
“Uptake” InterVapor System
TW: “奧提克”支氣管鏡蒸氣治療系統
Taiwan·Risk Class 2·MD·Uptake Medical B.V.·Registered Aug 06, 2020 – Aug 06, 2025ExpiredRegistration details
- Analysis ID
- ff2b8e9ec2bb05598cc0f3fc65d72aae
- License Form
- Ministry of Health Medical Device Import No. 033670
- Customs Code
- DHA05603367005
Company information
- Manufacturer
- Uptake Medical B.V.
- Manufacturer Country
- Netherlands
- Authorized Representative
- ERA BIOTEQ ENTERPRISE CO., LTD.
Product details
- Intended Use
- The InterVapor system is suitable for the treatment of patients with heterogeneous emphysema and hot water vapor therapy for the most severely ill lung segments to achieve bronchoscopic lung volume reduction.
- Product Type (Level 1)
- G ENT device
- Product Type (Level 2)
- G9999 Other
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Aug 06, 2020
- Expiry Date
- Aug 06, 2025
About this record
Access comprehensive regulatory information for “Uptake” InterVapor System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number ff2b8e9ec2bb05598cc0f3fc65d72aae and manufactured by Uptake Medical B.V.. The authorized representative in Taiwan is ERA BIOTEQ ENTERPRISE CO., LTD..
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