Taiwan FDA registration 9af511eac4b6cfac87c2dd6ec16c9c33
“Applied” Voyant Fine Fusion Device
TW: “安培”精細式組織凝結刀
Taiwan·Risk Class 2·MD·APPLIED MEDICAL RESOURCES CORPORATION·Registered Oct 31, 2022 – Oct 31, 2027ActiveRegistration details
- Analysis ID
- 9af511eac4b6cfac87c2dd6ec16c9c33
- License Form
- Ministry of Health Medical Device Import No. 036020
- Customs Code
- DHA05603602007
Company information
- Manufacturer
- APPLIED MEDICAL RESOURCES CORPORATION
- Manufacturer Country
- United States
- Authorized Representative
- DOUBLE-SUCCESS 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)
- I4400 Electric knife for cutting and hemostasis and its accessories
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Oct 31, 2022
- Expiry Date
- Oct 31, 2027
About this record
Access comprehensive regulatory information for “Applied” Voyant Fine Fusion Device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 9af511eac4b6cfac87c2dd6ec16c9c33 and manufactured by APPLIED MEDICAL RESOURCES CORPORATION. The authorized representative in Taiwan is DOUBLE-SUCCESS CO., LTD..
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