Taiwan FDA registration 439332d5b8b75485baaa830bda989cb0
"Maikewei" ultrasonic cutting hemostatic knife system
TW: “邁科唯”超音波切割止血刀系統
Registration details
- Analysis ID
- 439332d5b8b75485baaa830bda989cb0
- Customs Code
- DHA09200149808
Company information
- Manufacturer
- Miconvey Technologies Co., Ltd.
- Manufacturer Country
- China
- Authorized Representative
- KUAN FWA MED CO., LTD.
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I.0003 Ultrasound surgical device
- Import Information
- Chinese goods;; input
Dates and status
- Registration Date
- Dec 04, 2023
- Expiry Date
- Dec 04, 2028
About this record
Access comprehensive regulatory information for "Maikewei" ultrasonic cutting hemostatic knife system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 439332d5b8b75485baaa830bda989cb0 and manufactured by Miconvey Technologies Co., Ltd.. The authorized representative in Taiwan is KUAN FWA MED CO., LTD..
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
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