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“Heine” Direct Ophthalmoscope and Accessories - Taiwan Registration 5bdce0d8d253833ea8f49a7beb6a8611

Access comprehensive regulatory information for “Heine” Direct Ophthalmoscope 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 5bdce0d8d253833ea8f49a7beb6a8611 and manufactured by HEINE OPTOTECHNIK GMBH & CO. KG. The authorized representative in Taiwan is DENSO SCIENTIFIC 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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5bdce0d8d253833ea8f49a7beb6a8611
Registration Details
Taiwan FDA Registration: 5bdce0d8d253833ea8f49a7beb6a8611
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Device Details

“Heine” Direct Ophthalmoscope and Accessories
TW: “海尼恩” 直接眼底鏡及附件
Risk Class 2
MD

Registration Details

5bdce0d8d253833ea8f49a7beb6a8611

Ministry of Health Medical Device Import No. 027450

DHA05602745005

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

Jul 08, 2015

Jul 08, 2025