Pure Global

"Dr. Len" intraocular lens eyeball - Taiwan Registration 8b46c3ac329f8a8d3962f6579ff8b951

Access comprehensive regulatory information for "Dr. Len" intraocular lens eyeball in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 8b46c3ac329f8a8d3962f6579ff8b951 and manufactured by BAUSCH & LOMB INC.. The authorized representative in Taiwan is BAUSCH & LOMB TAIWAN LIMITED.

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
8b46c3ac329f8a8d3962f6579ff8b951
Registration Details
Taiwan FDA Registration: 8b46c3ac329f8a8d3962f6579ff8b951
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

"Dr. Len" intraocular lens eyeball
TW: "ๅšๅฃซๅ€ซ"ไบบๅทฅๆฐดๆ™ถ้ซ”็œผ็ƒ
Risk Class 2
Cancelled

Registration Details

8b46c3ac329f8a8d3962f6579ff8b951

DHA00600917208

Company Information

United States

Product Details

0314 Intraocular lens

import

Dates and Status

May 27, 1999

Feb 09, 2019

May 19, 2022

Cancellation Information

Logged out

่‡ช่กŒ้ตๅ…ฅ