Taiwan FDA registration 2ef5c62a43092350db47bc46b9e629ca

"Lotto" IOL Guide (Unsterilized)　

TW: “樂透”人工水晶體導引器 (未滅菌)　

Taiwan·Risk Class 1·PT ROHTO LABORATORIES INDONESIA·Registered Sep 15, 2009 – Sep 15, 2024Expired

Registration details

Analysis ID: 2ef5c62a43092350db47bc46b9e629ca
Customs Code: DHA04400810100

Company information

Manufacturer: PT ROHTO LABORATORIES INDONESIA
Manufacturer Country: Indonesia
Authorized Representative: SHIN SHENG PHARMACEUTICAL CO., LTD.

Product details

Intended Use: Limited to the first level identification range of "intraocular lens guide (M.4300)" of the Classification and Grading Management Measures for Medical Equipment.
Product Type (Level 1): M Ophthalmology
Product Type (Level 2): M.4300 Artificial crystal body inducer
Import Information: import

Dates and status

Registration Date: Sep 15, 2009
Expiry Date: Sep 15, 2024

About this record

Access comprehensive regulatory information for "Lotto" IOL Guide (Unsterilized)　 in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 2ef5c62a43092350db47bc46b9e629ca and manufactured by PT ROHTO LABORATORIES INDONESIA. The authorized representative in Taiwan is SHIN SHENG PHARMACEUTICAL CO., LTD..

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.