Taiwan FDA registration 003c9dbc754f15bf4fd14b40c83280cf
"Case" Artes Rubidium Chromium Skin Laser
TW: "況特" 亞瑟士銣雅鉻皮膚科雷射
Registration details
- Analysis ID
- 003c9dbc754f15bf4fd14b40c83280cf
- Customs Code
- DHA00601067406
Company information
- Manufacturer
- QUANTEL MEDICAL
- Manufacturer Country
- France
- Authorized Representative
- TAIWAN HWA IN ENTERPRISE CO., LTD.
Product details
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Import Information
- import
Dates and status
- Registration Date
- May 31, 2004
- Expiry Date
- May 31, 2009
- Cancellation Date
- Nov 16, 2012
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Case" Artes Rubidium Chromium Skin Laser in Taiwan's medical device market through Pure Global AI's free database. is registered under number 003c9dbc754f15bf4fd14b40c83280cf and manufactured by QUANTEL MEDICAL. The authorized representative in Taiwan is TAIWAN HWA IN ENTERPRISE CO., LTD..
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