Taiwan FDA registration 62b77417644dacf94ae31f122a10b698
"Rodun" new vision flexible intraocular lens
TW: “樂敦”新視軟式人工水晶體
Taiwan·Risk Class 3·PT. ROHTO LABORATORIES INDONESIA·Registered Sep 03, 2009 – Sep 03, 2029ActiveRegistration details
- Analysis ID
- 62b77417644dacf94ae31f122a10b698
- Customs Code
- DHA00602016402
Company information
- Manufacturer
- PT. ROHTO LABORATORIES INDONESIA
- Manufacturer Country
- Indonesia
- Authorized Representative
- SHIN SHENG PHARMACEUTICAL CO., LTD.
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.3600 Artificial Crystal
- Import Information
- import
Dates and status
- Registration Date
- Sep 03, 2009
- Expiry Date
- Sep 03, 2029
About this record
Access comprehensive regulatory information for "Rodun" new vision flexible intraocular lens in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 62b77417644dacf94ae31f122a10b698 and manufactured by PT. ROHTO LABORATORIES INDONESIA. The authorized representative in Taiwan is SHIN SHENG PHARMACEUTICAL 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