Taiwan FDA registration 0041144e1b7a0591b4fe89ba68ecefe8
Esstein Multi-Trabecular Micro-Diversion Stent System
TW: 愛視坦 多發式小樑微導流支架系統
Taiwan·Risk Class 2·GLAUKOS CORPORATION·Registered Oct 14, 2023 – Oct 14, 2028ActiveRegistration details
- Analysis ID
- 0041144e1b7a0591b4fe89ba68ecefe8
- Customs Code
- DHA05603663008
Company information
- Manufacturer
- GLAUKOS CORPORATION
- Manufacturer Country
- United States
- Authorized Representative
- QUALTECH CONSULTING CORPORATION
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- M Ophthalmology
- Product Type (Level 2)
- M.3920 Aqueous aqueous veil implants
- Import Information
- import
Dates and status
- Registration Date
- Oct 14, 2023
- Expiry Date
- Oct 14, 2028
About this record
Access comprehensive regulatory information for Esstein Multi-Trabecular Micro-Diversion Stent System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 0041144e1b7a0591b4fe89ba68ecefe8 and manufactured by GLAUKOS CORPORATION. The authorized representative in Taiwan is QUALTECH CONSULTING CORPORATION.
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