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"San Nishimura" Trial Lens Set (Non-Sterile) - Taiwan Registration 2fef3ba64a19e4a540f2b3395a430eff

Access comprehensive regulatory information for "San Nishimura" Trial Lens Set (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 2fef3ba64a19e4a540f2b3395a430eff and manufactured by SAN NISHIMURA CO., LTD.. 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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2fef3ba64a19e4a540f2b3395a430eff
Registration Details
Taiwan FDA Registration: 2fef3ba64a19e4a540f2b3395a430eff
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Device Details

"San Nishimura" Trial Lens Set (Non-Sterile)
TW: "ๆก‘ๅฐผ่ฅฟๅง†็ด" ่ฉฆ้ก็ต„ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

2fef3ba64a19e4a540f2b3395a430eff

Ministry of Health Medical Device Import No. 016787

DHA09401678700

Company Information

Japan

Product Details

Limited to the first level recognition range of the ophthalmic test lens group (M.1405) of the Measures for the Administration of Medical Devices.

M Ophthalmic devices

M1405 Ophthalmic Test Lens Group

Imported from abroad

Dates and Status

Jul 15, 2016

Jul 15, 2021