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"Rekai" portable tonometry pen - Taiwan Registration d4ad3dd3d261cdddd1fbba09bbcd9931

Access comprehensive regulatory information for "Rekai" portable tonometry pen in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d4ad3dd3d261cdddd1fbba09bbcd9931 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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d4ad3dd3d261cdddd1fbba09bbcd9931
Registration Details
Taiwan FDA Registration: d4ad3dd3d261cdddd1fbba09bbcd9931
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Device Details

"Rekai" portable tonometry pen
TW: โ€œ็‘žๅ‡ฑโ€ๆ”œๅธถๅผ็œผๅฃ“ๆธฌๅฎš็ญ†
Risk Class 2

Registration Details

d4ad3dd3d261cdddd1fbba09bbcd9931

DHA00601798700

Company Information

United States

Product Details

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

M Ophthalmology

M.1930 Eye Pressure Meter and its accessories

import

Dates and Status

Apr 04, 2007

Apr 04, 2027