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“LAFAYETTE” PERIMETER (Non-Sterile) - Taiwan Registration 493360bfa51dbff03d698bf9d45a0d80

Access comprehensive regulatory information for “LAFAYETTE” PERIMETER (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 493360bfa51dbff03d698bf9d45a0d80 and manufactured by LAFAYETTE INSTRUMENT COMPANY. The authorized representative in Taiwan is TODAY'S INSTRUMENTS CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including LAFAYETTE INSTRUMENT COMPANY, 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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493360bfa51dbff03d698bf9d45a0d80
Registration Details
Taiwan FDA Registration: 493360bfa51dbff03d698bf9d45a0d80
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Device Details

“LAFAYETTE” PERIMETER (Non-Sterile)
TW: “拉法葉” 視野計 (未滅菌)
Risk Class 1
MD
Cancelled

Registration Details

493360bfa51dbff03d698bf9d45a0d80

Ministry of Health Medical Device Import No. 021924

DHA09402192401

Company Information

United States

Product Details

M Ophthalmic devices

M1605 field of view mirror

Imported from abroad

Dates and Status

Sep 02, 2020

Sep 02, 2025

Cancellation Information

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