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“Lumendi” DiLumen Endolumenal Interventional Platform - Taiwan Registration 2a6715be7c1bb9f23a4afa7748f2aace

Access comprehensive regulatory information for “Lumendi” DiLumen Endolumenal Interventional Platform in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 2a6715be7c1bb9f23a4afa7748f2aace and manufactured by LUMENDI, LLC. The authorized representative in Taiwan is DOUBLE-SUCCESS CO., LTD..

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2a6715be7c1bb9f23a4afa7748f2aace
Registration Details
Taiwan FDA Registration: 2a6715be7c1bb9f23a4afa7748f2aace
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Device Details

“Lumendi” DiLumen Endolumenal Interventional Platform
TW: “羅曼迪”內視鏡手術通道
Risk Class 2
MD

Registration Details

2a6715be7c1bb9f23a4afa7748f2aace

Ministry of Health Medical Device Import No. 035370

DHA05603537003

Company Information

United States

Product Details

Details are as detailed as approved Chinese instructions

H Gastroenterology and urology

H1500 endoscope and accessories

Imported from abroad

Dates and Status

Mar 31, 2022

Mar 31, 2027