Taiwan FDA registration eefe087e7b6105257b51fb202915d415
“ARC” Diode Laser Wolf
TW: “亞爾斯”沃夫二極體雷射系統
Taiwan·Risk Class 2·MD·A.R.C. Laser GmbH·Registered Mar 09, 2023 – Mar 09, 2028ActiveRegistration details
- Analysis ID
- eefe087e7b6105257b51fb202915d415
- License Form
- Ministry of Health Medical Device Import No. 036431
- Customs Code
- DHA05603643102
Company information
- Manufacturer
- A.R.C. Laser GmbH
- Manufacturer Country
- Germany
- Authorized Representative
- PAXUAN CORPORATION
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)
- I4810 Lasers for general surgery, plastic surgery and dermatology
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Mar 09, 2023
- Expiry Date
- Mar 09, 2028
About this record
Access comprehensive regulatory information for “ARC” Diode Laser Wolf in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number eefe087e7b6105257b51fb202915d415 and manufactured by A.R.C. Laser GmbH. The authorized representative in Taiwan is PAXUAN CORPORATION.
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