Taiwan FDA registration b604182b81c2b7d06fc9a03417dd1a69
"Veli" double-lumen endobronchial tube
TW: “維立”雙腔支氣管內管
Taiwan·Risk Class 2·Well Lead Medical Co., Ltd.·Registered Nov 19, 2019 – Nov 19, 2029ActiveRegistration details
- Analysis ID
- b604182b81c2b7d06fc9a03417dd1a69
- Customs Code
- DHA09200108407
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
- Nov 19, 2019
- Expiry Date
- Nov 19, 2029
About this record
Access comprehensive regulatory information for "Veli" double-lumen endobronchial tube in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number b604182b81c2b7d06fc9a03417dd1a69 and manufactured by Well Lead Medical Co., Ltd.. The authorized representative in Taiwan is TAIWAN MEDICAL SERVICES CORPORATION.
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