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"NIDEK" Perimeter (Non-sterile) - Taiwan Registration 8a387c06d796dc5408ddede2ef82de1d

Access comprehensive regulatory information for "NIDEK" 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 8a387c06d796dc5408ddede2ef82de1d and manufactured by NIDEK CO., LTD. HAMACHO PLANT. The authorized representative in Taiwan is IKI MEDICAL CO., LTD..

This page provides complete technical specifications, regulatory compliance details. 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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8a387c06d796dc5408ddede2ef82de1d
Registration Details
Taiwan FDA Registration: 8a387c06d796dc5408ddede2ef82de1d
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Device Details

"NIDEK" Perimeter (Non-sterile)
TW: "ๅฐผๅพทๅ…‹" ่ฆ–้‡Ž่จˆ (ๆœชๆป…่Œ)
Risk Class 1
MD
Cancelled

Registration Details

8a387c06d796dc5408ddede2ef82de1d

Ministry of Health Medical Device Import No. 015397

DHA09401539705

Company Information

Product Details

M Ophthalmic devices

M1605 field of view mirror

Imported from abroad

Dates and Status

Jun 30, 2015

Jun 30, 2020

Aug 05, 2022

Cancellation Information

Logged out

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