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“NeoMedic” MINIMALLY INVASIVE PROLAPSE SYSTEM - Taiwan Registration 02291c65c883587dfa5044b419f30108

Access comprehensive regulatory information for “NeoMedic” MINIMALLY INVASIVE PROLAPSE SYSTEM in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 02291c65c883587dfa5044b419f30108 and manufactured by Desarrollo e Investigación Médica Aragonesa S.L.. The authorized representative in Taiwan is Soar Medical Corp..

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02291c65c883587dfa5044b419f30108
Registration Details
Taiwan FDA Registration: 02291c65c883587dfa5044b419f30108
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Device Details

“NeoMedic” MINIMALLY INVASIVE PROLAPSE SYSTEM
TW: “尼奧麥迪克”蜜普思微創骨盆懸吊系統
Risk Class 3
MD

Registration Details

02291c65c883587dfa5044b419f30108

Ministry of Health Medical Device Import No. 030820

DHA05603082009

Company Information

Product Details

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

l Devices for obstetrics and gynecology

L5980 Surgical mesh for transvaginal pelvic organ prolapse treatment

Imported from abroad

Dates and Status

Apr 25, 2018

Apr 25, 2028