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Wilden electronic sphygmomanometer - Taiwan Registration bca7d293238e659b500f1b852245a6b6

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 bca7d293238e659b500f1b852245a6b6 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, 1 companies making similar products including GMC Inc., 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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Registration Details
Taiwan FDA Registration: bca7d293238e659b500f1b852245a6b6
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Device Details

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

Registration Details

bca7d293238e659b500f1b852245a6b6

DHA09200073300

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

Dec 24, 2015

Dec 24, 2020

Jun 22, 2022

Cancellation Information

Logged out

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