Taiwan FDA registration 6db5a04d999c82b9a53ecfe25c25aef2

"Eye Care" Tian Shiming monolithic multifocal intraocular lens

TW: “眼力健”添視明單片型多焦點人工水晶體
Taiwan flagTaiwan·Risk Class 3·Johnson & Johnson surgical Vision, Inc.;; AMO PUERTO RICO MANUFACTURING, INC.·Registered May 27, 2010 – May 27, 2030Active
Registration details
Analysis ID
6db5a04d999c82b9a53ecfe25c25aef2
Customs Code
DHA00602106008
Company information
Manufacturer Country
United States
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.3600 Artificial Crystal
Import Information
import
Dates and status
Registration Date
May 27, 2010
Expiry Date
May 27, 2030
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About this record

Access comprehensive regulatory information for "Eye Care" Tian Shiming monolithic multifocal 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 6db5a04d999c82b9a53ecfe25c25aef2 and manufactured by Johnson & Johnson surgical Vision, Inc.;; AMO PUERTO RICO MANUFACTURING, INC.. The authorized representative in Taiwan is AMO ASIA LIMITED, TAIWAN BRANCH (HONG KONG).

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including Johnson & Johnson Surgical Vision, Inc.;; AMO PUERTO RICO MANUFACTURING, INC., and 1 recent registrations in the same category. 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.

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