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Dr. Pulse electronic blood pressure monitor - Taiwan Registration 02f2426ccf857d226fb7541fc7d0fd24

Access comprehensive regulatory information for Dr. Pulse electronic blood pressure monitor in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 02f2426ccf857d226fb7541fc7d0fd24 and manufactured by GMC Inc.. The authorized representative in Taiwan is ROSSMAX INTERNATIONAL LTD..

This page provides complete technical specifications, regulatory compliance details, 3 companies making similar products including ROSSMAX (SHANGHAI) INCORPORATION LTD, Yousheng Medical Technology Co., Ltd. Neihu No. 2 Factory, 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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02f2426ccf857d226fb7541fc7d0fd24
Registration Details
Taiwan FDA Registration: 02f2426ccf857d226fb7541fc7d0fd24
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Device Details

Dr. Pulse electronic blood pressure monitor
TW: ่„ˆๅšๅฃซ้›ปๅญ่ก€ๅฃ“่จˆ
Risk Class 2

Registration Details

02f2426ccf857d226fb7541fc7d0fd24

DHA09200105309

Company Information

China

Product Details

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

E Cardiovascular Medicine Science

E.1130.

Input;; Chinese goods

Dates and Status

Jul 25, 2019

Jul 25, 2029