Taiwan FDA registration f1845105f249180c7f94d5a16d74e65b

"Wonder" Soluti Ophthalmic Laser Photocoagulator

TW: “況特”索魯堤眼科雷射光凝儀
Taiwan flagTaiwan·Risk Class 2·QUANTEL MEDICAL·Registered Nov 24, 2011 – Nov 24, 2026Active
Registration details
Analysis ID
f1845105f249180c7f94d5a16d74e65b
Customs Code
DHA00602302901
Company information
Manufacturer
QUANTEL MEDICAL
Manufacturer Country
France
Authorized Representative
TAIWAN HWA IN ENTERPRISE 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.4390 眼科雷射裝置
Import Information
import
Dates and status
Registration Date
Nov 24, 2011
Expiry Date
Nov 24, 2026
About this record

Access comprehensive regulatory information for "Wonder" Soluti Ophthalmic Laser Photocoagulator in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number f1845105f249180c7f94d5a16d74e65b and manufactured by QUANTEL MEDICAL. 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