Taiwan FDA registration 7d93d94fb94a8685dedbebf422c88dee
"Velit" single-lumen endobronchial tube is used at one time
TW: “維立”一次性使用單腔支氣管內管
Taiwan·Risk Class 2·WELL LEAD MEDICAL CO., LTD.·Registered Jan 03, 2020 – Jan 03, 2025ExpiredRegistration details
- Analysis ID
- 7d93d94fb94a8685dedbebf422c88dee
- Customs Code
- DHA09200109907
Company information
- Manufacturer
- WELL LEAD MEDICAL CO., LTD.
- Manufacturer Country
- China
- Authorized Representative
- TAIWAN MEDICAL SERVICES CORPORATION
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.5740 Gas pipe/bronchi divergence gas line
- Import Information
- Chinese goods;; input
Dates and status
- Registration Date
- Jan 03, 2020
- Expiry Date
- Jan 03, 2025
About this record
Access comprehensive regulatory information for "Velit" single-lumen endobronchial tube is used at one time in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 7d93d94fb94a8685dedbebf422c88dee and manufactured by WELL LEAD MEDICAL CO., LTD.. The authorized representative in Taiwan is TAIWAN MEDICAL SERVICES CORPORATION.
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