Taiwan FDA registration 4ac75467b393a675cc055173efd34596
"Tampa" single-use double-lumen bronchial intubation
TW: “坦帕”一次性使用雙腔支氣管插管
Taiwan·Risk Class 2·Hangzhou Tappa Medical Technology Co., Ltd.·Registered Sep 09, 2019 – Sep 09, 2024ExpiredRegistration details
- Analysis ID
- 4ac75467b393a675cc055173efd34596
- Customs Code
- DHA09200106503
Company information
- Manufacturer
- Hangzhou Tappa Medical Technology Co., Ltd.
- Manufacturer Country
- China
- Authorized Representative
- BIOTRONIC INSTRUMENT ENTERPRISE LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- D Anesthesiology
- Product Type (Level 2)
- D.5720 Bronchi inner pipe
- Import Information
- Chinese goods;; input
Dates and status
- Registration Date
- Sep 09, 2019
- Expiry Date
- Sep 09, 2024
About this record
Access comprehensive regulatory information for "Tampa" single-use double-lumen bronchial intubation in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 4ac75467b393a675cc055173efd34596 and manufactured by Hangzhou Tappa Medical Technology Co., Ltd.. The authorized representative in Taiwan is BIOTRONIC INSTRUMENT ENTERPRISE LTD..
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