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)
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