Taiwan FDA registration d8f6a1e7cd0afdfb6be5c76cf7f697df
“Applied” Voyant 5mm & Maryland Fusion Device
TW: “安培”5mm及馬里蘭式組織凝結刀
Registration details
- Analysis ID
- d8f6a1e7cd0afdfb6be5c76cf7f697df
- License Form
- Ministry of Health Medical Device Import No. 035848
- Customs Code
- DHA05603584804
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
- Sep 15, 2022
- Expiry Date
- Sep 15, 2027
About this record
Access comprehensive regulatory information for “Applied” Voyant 5mm & Maryland 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 d8f6a1e7cd0afdfb6be5c76cf7f697df and manufactured by APPLIED MEDICAL RESOURCES CORPORATION. The authorized representative in Taiwan is DOUBLE-SUCCESS 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.
Free DatabasePowered by Pure Global AI89,000+ Devices