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"IDMED NeuroLight" Pupillometer (Non-Sterile) - Taiwan Registration 420df813c222ffd6544a653fd3af2fc7

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 420df813c222ffd6544a653fd3af2fc7 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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420df813c222ffd6544a653fd3af2fc7
Registration Details
Taiwan FDA Registration: 420df813c222ffd6544a653fd3af2fc7
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Device Details

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

Registration Details

420df813c222ffd6544a653fd3af2fc7

Ministry of Health Medical Device Import No. 021298

DHA09402129802

Company Information

France

Product Details

M Ophthalmic devices

M1700 Pupillometer

Imported from abroad

Dates and Status

Feb 20, 2020

Feb 20, 2025

Cancellation Information

Logged out

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