Taiwan FDA registration 2cd81bed5fe64fee3cbe02c6d762ae2d
"Seton" Puferno laser system
TW: “賽頓”普費諾雷射系統
Taiwan·Risk Class 2·SCITON, INC.·Registered Jul 10, 2008 – Jul 10, 2018CancelledRegistration details
- Analysis ID
- 2cd81bed5fe64fee3cbe02c6d762ae2d
- Customs Code
- DHA00601910400
Company information
- Manufacturer
- SCITON, INC.
- Manufacturer Country
- United States
- Authorized Representative
- DYNAMIC MEDICAL TECHNOLOGIES INC.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- 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
- import
Dates and status
- Registration Date
- Jul 10, 2008
- Expiry Date
- Jul 10, 2018
- Cancellation Date
- Jun 07, 2022
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Seton" Puferno laser system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 2cd81bed5fe64fee3cbe02c6d762ae2d and manufactured by SCITON, INC.. The authorized representative in Taiwan is DYNAMIC MEDICAL TECHNOLOGIES INC..
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