Taiwan FDA registration a57ad941110c6fbf88b9d3558bb13dcd
"Big Boat" Oroman diode laser system
TW: “大舟”奧羅馬二極體雷射系統
Taiwan·Risk Class 2·DAEJU MEDITECH ENGINEERING Co., Ltd.·Registered Sep 30, 2024 – Sep 30, 2029ActiveRegistration details
- Analysis ID
- a57ad941110c6fbf88b9d3558bb13dcd
- Customs Code
- DHA05603760909
Company information
- Manufacturer
- DAEJU MEDITECH ENGINEERING Co., Ltd.
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- Peiruixing Biotechnology Co., Ltd
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
- import
Dates and status
- Registration Date
- Sep 30, 2024
- Expiry Date
- Sep 30, 2029
About this record
Access comprehensive regulatory information for "Big Boat" Oroman diode 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 a57ad941110c6fbf88b9d3558bb13dcd and manufactured by DAEJU MEDITECH ENGINEERING Co., Ltd.. The authorized representative in Taiwan is Peiruixing Biotechnology 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