Taiwan FDA registration 48574b35e6cb783d7fb9d022e70c10b7
“MEGADYNE” ACE BLADE 700
TW: “美佳泰”王牌外科電刀筆
Taiwan·Risk Class 2·MD·Megadyne Medical Products, Inc.·Registered Dec 30, 2019 – Dec 30, 2024ExpiredRegistration details
- Analysis ID
- 48574b35e6cb783d7fb9d022e70c10b7
- License Form
- Ministry of Health Medical Device Import No. 033149
- Customs Code
- DHA05603314907
Company information
- Manufacturer
- Megadyne Medical Products, Inc.
- Manufacturer Country
- United States
- Authorized Representative
- JOHNSON & JOHNSON MEDICAL TAIWAN LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- I General and plastic surgical devices
- Product Type (Level 2)
- I4400 Electric knife for cutting and hemostasis and its accessories
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Dec 30, 2019
- Expiry Date
- Dec 30, 2024
About this record
Access comprehensive regulatory information for “MEGADYNE” ACE BLADE 700 in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 48574b35e6cb783d7fb9d022e70c10b7 and manufactured by Megadyne Medical Products, Inc.. The authorized representative in Taiwan is JOHNSON & JOHNSON MEDICAL TAIWAN 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