Taiwan FDA registration 1e8b4e8ea290a808631029eb1dc902b0
"Medicel" Intraocular lens guide (Non-Sterile)
TW: "梅地斯" 人工水晶體導引器 (未滅菌)
Registration details
- Analysis ID
- 1e8b4e8ea290a808631029eb1dc902b0
- License Form
- Ministry of Health Medical Device Import No. 013562
- Customs Code
- DHA09401356200
Company information
- Manufacturer
- MEDICEL AG
- Manufacturer Country
- Switzerland
- Authorized Representative
- TAIWAN HWA IN ENTERPRISE CO., LTD.
Product details
- Intended Use
- Limited to the first level identification range of "Intraocular Lens Guide (M.4300)" under the Measures for the Administration of Medical Equipment.
- Product Type (Level 1)
- M Ophthalmic devices
- Product Type (Level 2)
- M4300 Intraocular Lens Guide
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Nov 06, 2013
- Expiry Date
- Nov 06, 2023
About this record
Access comprehensive regulatory information for "Medicel" Intraocular lens guide (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 1e8b4e8ea290a808631029eb1dc902b0 and manufactured by MEDICEL AG. The authorized representative in Taiwan is TAIWAN HWA IN ENTERPRISE CO., LTD..
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