Pure Global

"Ostic" Atifix intraocular lens - Taiwan Registration 1b14de22e2044b4b77ce0611062f729f

Access comprehensive regulatory information for "Ostic" Atifix intraocular lens in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 1b14de22e2044b4b77ce0611062f729f and manufactured by OPHTEC B.V.. The authorized representative in Taiwan is BUTICON INTERNATIONAL CORPORATION.

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 Database
Powered by Pure Global AI
89,000+ Devices
1b14de22e2044b4b77ce0611062f729f
Registration Details
Taiwan FDA Registration: 1b14de22e2044b4b77ce0611062f729f
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

"Ostic" Atifix intraocular lens
TW: โ€œๆญๆ–ฏๆๅ…‹โ€้˜ฟๆ่ฒๅ…‹ๆ–ฏไบบๅทฅๆฐดๆ™ถ้ซ”
Risk Class 3

Registration Details

1b14de22e2044b4b77ce0611062f729f

DHA00602112102

Company Information

Netherlands

Product Details

For details, it is Chinese approved copy of the imitation order

M Ophthalmology

M.3600 Artificial Crystal

import

Dates and Status

Jun 11, 2010

Jun 11, 2025