Pure Global

"Nidek" non-contact tonometer / corneal thickness measuring instrument - Taiwan Registration 9515ccc7b9d234d81be5e53a680a32f0

Access comprehensive regulatory information for "Nidek" non-contact tonometer / corneal thickness measuring instrument in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 9515ccc7b9d234d81be5e53a680a32f0 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.

Free Database
Powered by Pure Global AI
89,000+ Devices
9515ccc7b9d234d81be5e53a680a32f0
Registration Details
Taiwan FDA Registration: 9515ccc7b9d234d81be5e53a680a32f0
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

"Nidek" non-contact tonometer / corneal thickness measuring instrument
TW: โ€œๅฐผๅพทๅ…‹โ€้žๆŽฅ่งธๅผ็œผๅฃ“่จˆ/่ง’่†œๅŽšๅบฆๆธฌ้‡ๅ„€
Risk Class 2

Registration Details

9515ccc7b9d234d81be5e53a680a32f0

DHA00602086404

Company Information

Product Details

For details, it is Chinese approved copy of the imitation order

M Ophthalmology

M.1930 Eye Pressure Meter and its accessories

import

Dates and Status

Mar 29, 2010

Mar 29, 2030