Taiwan FDA registration a2c8165f3aedf17dd030bd9db82dd36b
"Veli" single-use with suction tube, endotracheal tube
TW: “維立”一次性使用帶抽痰管氣管內管
Taiwan·Risk Class 2·Well Lead Medical Co., Ltd.·Registered Jan 16, 2020 – Jan 16, 2025ExpiredRegistration details
- Analysis ID
- a2c8165f3aedf17dd030bd9db82dd36b
- Customs Code
- DHA09200110400
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.5730 Endotracheal tubes
- Import Information
- Chinese goods;; input
Dates and status
- Registration Date
- Jan 16, 2020
- Expiry Date
- Jan 16, 2025
About this record
Access comprehensive regulatory information for "Veli" single-use with suction tube, endotracheal tube in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number a2c8165f3aedf17dd030bd9db82dd36b and manufactured by Well Lead Medical Co., Ltd.. The authorized representative in Taiwan is TAIWAN MEDICAL SERVICES CORPORATION.
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