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“Reichert” Ocular Response Analyzer - Taiwan Registration 8676c081a93447cf47ecaf21b277c23e

Access comprehensive regulatory information for “Reichert” Ocular Response Analyzer in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 8676c081a93447cf47ecaf21b277c23e and manufactured by REICHERT, INC.. The authorized representative in Taiwan is Kang Cheng Medical Technology Co., Ltd.

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8676c081a93447cf47ecaf21b277c23e
Registration Details
Taiwan FDA Registration: 8676c081a93447cf47ecaf21b277c23e
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Device Details

“Reichert” Ocular Response Analyzer
TW: “瑞凱”角膜生物力學反應分析儀
Risk Class 2
MD

Registration Details

8676c081a93447cf47ecaf21b277c23e

Ministry of Health Medical Device Import No. 033058

DHA05603305804

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

Dec 07, 2019

Dec 07, 2024