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Dr. Pulse electronic blood pressure monitor - Taiwan Registration f9b29137d360534831fa5f7b1945e720

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 f9b29137d360534831fa5f7b1945e720 and manufactured by ROSSMAX (SHANGHAI) INCORPORATION LTD. The authorized representative in Taiwan is ROSSMAX INTERNATIONAL LTD..

This page provides complete technical specifications, regulatory compliance details, 3 companies making similar products including Yousheng Medical Technology Co., Ltd. Neihu No. 2 Factory, 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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f9b29137d360534831fa5f7b1945e720
Registration Details
Taiwan FDA Registration: f9b29137d360534831fa5f7b1945e720
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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

f9b29137d360534831fa5f7b1945e720

DHA04200037201

Company Information

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

Jun 21, 2011

Jun 21, 2021

Sep 23, 2023

Cancellation Information

Logged out

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