Taiwan FDA registration 420df813c222ffd6544a653fd3af2fc7

"IDMED NeuroLight" Pupillometer (Non-Sterile)

TW: "艾德美" 瞳孔計 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·IDMED·Registered Feb 20, 2020 – Feb 20, 2025Cancelled
Registration details
Analysis ID
420df813c222ffd6544a653fd3af2fc7
License Form
Ministry of Health Medical Device Import No. 021298
Customs Code
DHA09402129802
Company information
Manufacturer
IDMED
Manufacturer Country
France
Authorized Representative
DRAEGER MEDICAL TAIWAN LTD.
Product details
Product Type (Level 1)
M Ophthalmic devices
Product Type (Level 2)
M1700 Pupillometer
Import Information
Imported from abroad
Dates and status
Registration Date
Feb 20, 2020
Expiry Date
Feb 20, 2025
Cancellation information
Status
Logged out
Reason
轉為登錄字號
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About this record

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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