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Wilden electronic sphygmomanometer - Taiwan Registration ea637e00a50b65ba3f2adba958eb398a

Access comprehensive regulatory information for Wilden electronic sphygmomanometer in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number ea637e00a50b65ba3f2adba958eb398a and manufactured by GMC Inc.. The authorized representative in Taiwan is ROSSMAX INTERNATIONAL LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including Rossmax (Shanghai) Incorporation Ltd., and 1 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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ea637e00a50b65ba3f2adba958eb398a
Registration Details
Taiwan FDA Registration: ea637e00a50b65ba3f2adba958eb398a
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Device Details

Wilden electronic sphygmomanometer
TW: ๅจ็ˆพ็™ป้›ปๅญ่ก€ๅฃ“่จˆ
Risk Class 2

Registration Details

ea637e00a50b65ba3f2adba958eb398a

DHA09200119809

Company Information

China

Product Details

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

E Cardiovascular Medicine Science

E.1130.

Chinese goods;; input

Dates and Status

Feb 01, 2021

Jul 25, 2029

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