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)
Taiwan flagTaiwan·Risk Class 1·MD·MEDICEL AG·Registered Nov 06, 2013 – Nov 06, 2023Expired
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..

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