Taiwan FDA registration bca7d293238e659b500f1b852245a6b6

Wilden electronic sphygmomanometer

TW: 威爾登電子血壓計
Taiwan flagTaiwan·Risk Class 2·Rossmax (Shanghai) Incorporation Ltd.·Registered Dec 24, 2015 – Dec 24, 2020Cancelled
Registration details
Analysis ID
bca7d293238e659b500f1b852245a6b6
Customs Code
DHA09200073300
Company information
Manufacturer Country
China
Authorized Representative
ROSSMAX INTERNATIONAL LTD.
Product details
Intended Use
For details, it is Chinese approved copy of the imitation order
Product Type (Level 1)
E Cardiovascular Medicine Science
Product Type (Level 2)
E.1130.
Import Information
Chinese goods;; input
Dates and status
Registration Date
Dec 24, 2015
Expiry Date
Dec 24, 2020
Cancellation Date
Jun 22, 2022
Cancellation information
Status
Logged out
Reason
許可證已逾有效期
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About this record

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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