Taiwan FDA registration ea637e00a50b65ba3f2adba958eb398a

Wilden electronic sphygmomanometer

TW: 威爾登電子血壓計
Taiwan flagTaiwan·Risk Class 2·GMC Inc.·Registered Feb 01, 2021 – Jul 25, 2029Active
Registration details
Analysis ID
ea637e00a50b65ba3f2adba958eb398a
Customs Code
DHA09200119809
Company information
Manufacturer
GMC Inc.
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
Feb 01, 2021
Expiry Date
Jul 25, 2029
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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 ea637e00a50b65ba3f2adba958eb398a and manufactured by GMC Inc.. The authorized representative in Taiwan is ROSSMAX INTERNATIONAL LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including Rossmax (Shanghai) Incorporation Ltd., 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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