Taiwan FDA registration dd42284d1e37ae38cf1eec814fadce4b
“Asclepion” QuadroStarPRO Laser
TW: “阿斯克比恩”庫卓普羅雷射儀
Registration details
- Analysis ID
- dd42284d1e37ae38cf1eec814fadce4b
- License Form
- Ministry of Health Medical Device Import No. 026775
- Customs Code
- DHA05602677502
Company information
- Manufacturer
- Asclepion Laser Technologies GmbH
- Manufacturer Country
- Germany
- Authorized Representative
- QUALTECH CONSULTING 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
- Nov 06, 2014
- Expiry Date
- Nov 06, 2024
About this record
Access comprehensive regulatory information for “Asclepion” QuadroStarPRO Laser in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number dd42284d1e37ae38cf1eec814fadce4b and manufactured by Asclepion Laser Technologies GmbH. The authorized representative in Taiwan is QUALTECH CONSULTING 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