Taiwan FDA registration 37e6b8c5dbda088519083bd05098a824
"Umiko" Ni Orsis laser
TW: “優美克”妮傲西斯雷射儀
Taiwan·Risk Class 2·FINEMEC·Registered Jul 02, 2012 – Jul 02, 2017CancelledRegistration details
- Analysis ID
- 37e6b8c5dbda088519083bd05098a824
- Customs Code
- DHA00602369700
Company information
- Manufacturer
- FINEMEC
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- Yixin International Co., Ltd
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 02, 2012
- Expiry Date
- Jul 02, 2017
- Cancellation Date
- Dec 09, 2019
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Umiko" Ni Orsis laser in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 37e6b8c5dbda088519083bd05098a824 and manufactured by FINEMEC. The authorized representative in Taiwan is Yixin International 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