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TOMEY Auto Ref-Keratometer series(Non-Sterile) - Taiwan Registration f02d4b71140ed9d7c8faf666fe79f8e5

Access comprehensive regulatory information for TOMEY Auto Ref-Keratometer series(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 f02d4b71140ed9d7c8faf666fe79f8e5 and manufactured by TOMEY CORPORATION. The authorized representative in Taiwan is QUALTECH CONSULTING CORPORATION.

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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f02d4b71140ed9d7c8faf666fe79f8e5
Registration Details
Taiwan FDA Registration: f02d4b71140ed9d7c8faf666fe79f8e5
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Device Details

TOMEY Auto Ref-Keratometer series(Non-Sterile)
TW: "ๅคš็พŽ" ้›ป่…ฆ้ฉ—ๅ…‰ๅผงๅบฆๅ„€็ณปๅˆ—(ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

f02d4b71140ed9d7c8faf666fe79f8e5

Ministry of Health Medical Device Import Registration No. 003776

DHA08400377601

Company Information

Japan

Product Details

Limited to the first level recognition range of ophthalmic optometry machine (M.1760) of the management measures for medical equipment.

M Ophthalmic devices

M1760 Ophthalmic Refractive Machine

Imported from abroad

Dates and Status

Oct 01, 2021

Oct 31, 2026