Taiwan FDA registration 72183c264c4302624aac54353dec0b4a
"Dr. Lun" Dawning Advanced Ultrasound Emulsification System Surgical Kit and Its Accessories
TW: “博士倫”曙光進階超音波乳化系統手術包及其配件
Registration details
- Analysis ID
- 72183c264c4302624aac54353dec0b4a
- Customs Code
- DHA00602316101
Company information
- Manufacturer
- BAUSCH & LOMB INC.
- Manufacturer Country
- United States
- Authorized Representative
- BAUSCH & LOMB TAIWAN LIMITED
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- M Ophthalmology
- Product Type (Level 2)
- M.4670 Crystal emulsifier
- Import Information
- import
Dates and status
- Registration Date
- Jan 05, 2012
- Expiry Date
- Jan 05, 2027
About this record
Access comprehensive regulatory information for "Dr. Lun" Dawning Advanced Ultrasound Emulsification System Surgical Kit and Its Accessories in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 72183c264c4302624aac54353dec0b4a and manufactured by BAUSCH & LOMB INC.. The authorized representative in Taiwan is BAUSCH & LOMB TAIWAN 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