Taiwan FDA registration 21c9460d483be4be91ed2c1912adab0e
"Prowei" electric knife pen
TW: “普威”電刀筆
Registration details
- Analysis ID
- 21c9460d483be4be91ed2c1912adab0e
- Customs Code
- DHY00500346301
Company information
- Manufacturer
- Puwei International Co., Ltd. Yilan Factory
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- UNIMAX MEDICAL SYSTEMS INC.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I.4400 Cutting and hemostasis electric knives and accessories thereof
- Import Information
- Domestic
Dates and status
- Registration Date
- Sep 30, 2011
- Expiry Date
- Sep 30, 2026
About this record
Access comprehensive regulatory information for "Prowei" electric knife pen in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 21c9460d483be4be91ed2c1912adab0e and manufactured by Puwei International Co., Ltd. Yilan Factory. The authorized representative in Taiwan is UNIMAX MEDICAL SYSTEMS INC..
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