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“Reichert” Auto Tonometer - Taiwan Registration dbca6302c570aa798fb616ac15edb197

Access comprehensive regulatory information for “Reichert” Auto Tonometer in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number dbca6302c570aa798fb616ac15edb197 and manufactured by REICHERT, INC.. The authorized representative in Taiwan is TAIWAN HWA IN ENTERPRISE 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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dbca6302c570aa798fb616ac15edb197
Registration Details
Taiwan FDA Registration: dbca6302c570aa798fb616ac15edb197
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Device Details

“Reichert” Auto Tonometer
TW: “瑞凱”自動眼壓計
Risk Class 2
MD

Registration Details

dbca6302c570aa798fb616ac15edb197

Ministry of Health Medical Device Import No. 029787

DHA05602978701

Company Information

United States

Product Details

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

M Ophthalmic devices

M1930 Tonometer and accessories

Imported from abroad

Dates and Status

Jun 08, 2017

Jun 08, 2022