Taiwan FDA registration 38d9f0ac1af3aed77b399cc8cedb2380
“DERMACARE” EDISC Bipolar Electrode
TW: “德瑪凱”易速凝雙極電燒器
Taiwan·Risk Class 2·MD·DERMACARE BIOMED INC.·Registered Jan 13, 2021 – Jun 16, 2025ExpiredRegistration details
- Analysis ID
- 38d9f0ac1af3aed77b399cc8cedb2380
- License Form
- Ministry of Health Medical Device Manufacturing No. 007054
Company information
- Manufacturer
- DERMACARE BIOMED INC.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- DERMACARE BIOMED INC.
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
- Produced in Taiwan, China
Dates and status
- Registration Date
- Jan 13, 2021
- Expiry Date
- Jun 16, 2025
About this record
Access comprehensive regulatory information for “DERMACARE” EDISC Bipolar Electrode in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 38d9f0ac1af3aed77b399cc8cedb2380 and manufactured by DERMACARE BIOMED INC.. The authorized representative in Taiwan is DERMACARE BIOMED INC..
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