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"Takagi" Keratometer (Non-Sterile) - Taiwan Registration 3adfec006e75ef774441fcacc1962ed5

Access comprehensive regulatory information for "Takagi" Keratometer (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 3adfec006e75ef774441fcacc1962ed5 and manufactured by TAKAGI SEIKO CO., LTD.. The authorized representative in Taiwan is IKI MEDICAL CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including TAKAGI SEIKO CO., LTD., 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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3adfec006e75ef774441fcacc1962ed5
Registration Details
Taiwan FDA Registration: 3adfec006e75ef774441fcacc1962ed5
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Device Details

"Takagi" Keratometer (Non-Sterile)
TW: "้ซ˜ๆœจ็ฒพๅทฅ" ่ง’่†œๅผงๅบฆๅ„€ (ๆœชๆป…่Œ)
Risk Class 1
MD
Cancelled

Registration Details

3adfec006e75ef774441fcacc1962ed5

Ministry of Health Medical Device Import No. 015941

DHA09401594102

Company Information

Japan

Product Details

M Ophthalmic devices

M1350 Keatoscope

Imported from abroad

Dates and Status

Dec 07, 2015

Dec 07, 2020

Aug 05, 2022

Cancellation Information

Logged out

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