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Dr. Pulse electronic blood pressure monitor - Taiwan Registration 7d1e9610880e002ec3c5d34e48f1722d

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 7d1e9610880e002ec3c5d34e48f1722d and manufactured by Yousheng Medical Technology Co., Ltd. Neihu No. 2 Factory. 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, GMC Inc., 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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7d1e9610880e002ec3c5d34e48f1722d
Registration Details
Taiwan FDA Registration: 7d1e9610880e002ec3c5d34e48f1722d
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Device Details

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

Registration Details

7d1e9610880e002ec3c5d34e48f1722d

DHY00500307706

Company Information

Product Details

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

E Cardiovascular Medicine Science

E.1130.

Domestic

Dates and Status

Aug 16, 2010

Aug 16, 2025

Jul 10, 2020

Cancellation Information

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