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"Deutsche Boi" sphygmomanometer - Taiwan Registration 644fd58d26e2907c4256cb854bd762f7

Access comprehensive regulatory information for "Deutsche Boi" sphygmomanometer in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 644fd58d26e2907c4256cb854bd762f7 and manufactured by BEURER GMBH & CO.. The authorized representative in Taiwan is BIOWELL HEALTH & WELL-BEING INC..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including BEURER GMBH, and 3 recent registrations in the same category. 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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644fd58d26e2907c4256cb854bd762f7
Registration Details
Taiwan FDA Registration: 644fd58d26e2907c4256cb854bd762f7
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Device Details

"Deutsche Boi" sphygmomanometer
TW: โ€œๅพทๅœ‹ๅšไพโ€่ก€ๅฃ“่จˆ
Risk Class 2

Registration Details

644fd58d26e2907c4256cb854bd762f7

DHA00602090709

Company Information

Germany

Product Details

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

E Cardiovascular Medicine Science

E.1130.

import

Dates and Status

Apr 14, 2010

Apr 14, 2030

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