Taiwan FDA registration c9824b8284ff344303a98b0f4aa9b3bf
“DENMAT SOL” Portable Diode Laser
TW: 登美可攜式二極體雷射
Taiwan·Risk Class 2·MD·DEN-MAT HOLDINGS, LLC·Registered Jan 17, 2017 – Jan 17, 2022CancelledRegistration details
- Analysis ID
- c9824b8284ff344303a98b0f4aa9b3bf
- License Form
- Ministry of Health Medical Device Import No. 029346
- Customs Code
- DHA05602934607
Company information
- Manufacturer
- DEN-MAT HOLDINGS, LLC
- Manufacturer Country
- United States
- Authorized Representative
- AIREX CORP.
Product details
- 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 17, 2017
- Expiry Date
- Jan 17, 2022
- Cancellation Date
- May 05, 2022
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for “DENMAT SOL” Portable 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 c9824b8284ff344303a98b0f4aa9b3bf and manufactured by DEN-MAT HOLDINGS, LLC. The authorized representative in Taiwan is AIREX CORP..
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