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"IDMED NeuroLight" Pupillometer (Non-Sterile) - Taiwan Registration 4f3984c003ccf5070d3b357e61e417d3

Access comprehensive regulatory information for "IDMED NeuroLight" Pupillometer (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 4f3984c003ccf5070d3b357e61e417d3 and manufactured by IDMED. The authorized representative in Taiwan is DRAEGER MEDICAL TAIWAN LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including IDMED, 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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4f3984c003ccf5070d3b357e61e417d3
Registration Details
Taiwan FDA Registration: 4f3984c003ccf5070d3b357e61e417d3
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Device Details

"IDMED NeuroLight" Pupillometer (Non-Sterile)
TW: "่‰พๅพท็พŽ" ็žณๅญ”่จˆ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

4f3984c003ccf5070d3b357e61e417d3

Ministry of Health Medical Device Import Registration No. 021298

DHA08402129806

Company Information

France

Product Details

Limited to the first level recognition range of the "Pupil Meter (M.1700)" of the Measures for the Administration of Medical Devices.

M Ophthalmic devices

M1700 Pupillometer

Imported from abroad

Dates and Status

Oct 01, 2021

Oct 31, 2025

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