Taiwan FDA registration 45cea813227f3c1834b44a57f2288976
“A.R.C.” Wolf Diode Laser
TW: “亞爾斯”沃夫二極體雷射系統
Taiwan·Risk Class 2·MD·A.R.C. LASER GMBH·Registered Jan 18, 2019 – Jan 18, 2029ActiveRegistration details
- Analysis ID
- 45cea813227f3c1834b44a57f2288976
- License Form
- Ministry of Health Medical Device Import No. 032213
- Customs Code
- DHA05603221301
Company information
- Manufacturer
- A.R.C. LASER GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- PAXUAN CORPORATION
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)
- I4810 Lasers for general surgery, plastic surgery and dermatology
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jan 18, 2019
- Expiry Date
- Jan 18, 2029
About this record
Access comprehensive regulatory information for “A.R.C.” Wolf Diode Laser in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 45cea813227f3c1834b44a57f2288976 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