Taiwan FDA registration 99e99884d75c655912e58f7af0306156

"Ophtec" Intraocular Lens Guide (non-sterile)

TW: "歐視得" 人工水晶體導引器 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·OPHTEC B.V.·Registered May 27, 2015 – May 27, 2025Expired
Registration details
Analysis ID
99e99884d75c655912e58f7af0306156
License Form
Ministry of Health Medical Device Import No. 015268
Customs Code
DHA09401526807
Company information
Manufacturer
OPHTEC B.V.
Manufacturer Country
Netherlands
Authorized Representative
UNITED MEDICAL INC.
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
May 27, 2015
Expiry Date
May 27, 2025
About this record

Access comprehensive regulatory information for "Ophtec" 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 99e99884d75c655912e58f7af0306156 and manufactured by OPHTEC B.V.. The authorized representative in Taiwan is UNITED MEDICAL INC..

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