Taiwan FDA registration d6bd94fbcd49fe447953a58ee70c6925
"Taiken" IOL guide (unsterilized)
TW: "大肯" 人工水晶體導引器 (未滅菌)
Taiwan·Risk Class 1·DUCKWORTH & KENT LTD·Registered Oct 25, 2006 – Oct 25, 2026ActiveRegistration details
- Analysis ID
- d6bd94fbcd49fe447953a58ee70c6925
- Customs Code
- DHA04400526808
Company information
- Manufacturer
- DUCKWORTH & KENT LTD
- Manufacturer Country
- United Kingdom
- Authorized Representative
- AMO ASIA LIMITED, TAIWAN BRANCH (HONG KONG)
Product details
- Intended Use
- Limited to the first level identification range of "intraocular lens guide (M.4300)" of the Classification and Grading Management Measures for Medical Equipment.
- Product Type (Level 1)
- M Ophthalmology
- Product Type (Level 2)
- M.4300 Artificial crystal body inducer
- Import Information
- import
Dates and status
- Registration Date
- Oct 25, 2006
- Expiry Date
- Oct 25, 2026
About this record
Access comprehensive regulatory information for "Taiken" IOL guide (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number d6bd94fbcd49fe447953a58ee70c6925 and manufactured by DUCKWORTH & KENT LTD. The authorized representative in Taiwan is AMO ASIA LIMITED, TAIWAN BRANCH (HONG KONG).
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