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“NEITZ” Direct Ophthalmoscopes and Accessories - Taiwan Registration 7728dae3176449fb9e10f7466c6c41c7

Access comprehensive regulatory information for “NEITZ” Direct Ophthalmoscopes and Accessories in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 7728dae3176449fb9e10f7466c6c41c7 and manufactured by NEITZ INSTRUMENTS CO., LTD.. The authorized representative in Taiwan is Kangcheng Biomedical Technology 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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7728dae3176449fb9e10f7466c6c41c7
Registration Details
Taiwan FDA Registration: 7728dae3176449fb9e10f7466c6c41c7
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Device Details

“NEITZ” Direct Ophthalmoscopes and Accessories
TW: “奈斯”直接眼底鏡及其配件
Risk Class 2
MD

Registration Details

7728dae3176449fb9e10f7466c6c41c7

Ministry of Health Medical Device Import No. 034221

DHA05603422107

Company Information

Product Details

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

M Ophthalmic devices

M1570 fundus mirror

Imported from abroad

Dates and Status

Dec 16, 2020

Dec 16, 2025