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“LAFAYETTE” PERIMETER (Non-Sterile) - Taiwan Registration b0c54441abfbc55afbb2ae96ee5105a0

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 b0c54441abfbc55afbb2ae96ee5105a0 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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b0c54441abfbc55afbb2ae96ee5105a0
Registration Details
Taiwan FDA Registration: b0c54441abfbc55afbb2ae96ee5105a0
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Device Details

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

Registration Details

b0c54441abfbc55afbb2ae96ee5105a0

Ministry of Health Medical Device Import Registration No. 021924

DHA08402192405

Company Information

United States

Product Details

Limited to the first-level identification range of the "Visual Field Scope (M.1605)" of the Measures for the Administration of Medical Equipment.

M Ophthalmic devices

M1605 field of view mirror

Imported from abroad

Dates and Status

Oct 01, 2021

Oct 31, 2025

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