Taiwan FDA registration 2d9895376c54d9e67ff0ac92d38a7fee
"Qin Sheng" helium-neon laser
TW: “覲晟”氦氖雷射
Taiwan·Risk Class 2·NEEDLELESS CORPORATION·Registered Mar 16, 2022 – Mar 16, 2027ActiveRegistration details
- Analysis ID
- 2d9895376c54d9e67ff0ac92d38a7fee
Company information
- Manufacturer
- NEEDLELESS CORPORATION
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- Jin-Cheng Medical Company Limited
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)
- I.4810 Lasers for general surgical, orthopaedic and dermatological use
- Import Information
- Contract manufacturing;; Domestic
Dates and status
- Registration Date
- Mar 16, 2022
- Expiry Date
- Mar 16, 2027
About this record
Access comprehensive regulatory information for "Qin Sheng" helium-neon laser in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 2d9895376c54d9e67ff0ac92d38a7fee and manufactured by NEEDLELESS CORPORATION. The authorized representative in Taiwan is Jin-Cheng Medical Company Limited.
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