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“Covidien” Parietex Optimized Composite Mesh - Taiwan Registration d7d285f9708c0e35970fa05965a3f54c

Access comprehensive regulatory information for “Covidien” Parietex Optimized Composite Mesh in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d7d285f9708c0e35970fa05965a3f54c and manufactured by SOFRADIM PRODUCTION. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) LTD..

This page provides complete technical specifications, regulatory compliance details. 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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d7d285f9708c0e35970fa05965a3f54c
Registration Details
Taiwan FDA Registration: d7d285f9708c0e35970fa05965a3f54c
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Device Details

“Covidien” Parietex Optimized Composite Mesh
TW: “柯惠”舒法定帕瑞德精優化合成網狀編網
Risk Class 2
MD
Cancelled

Registration Details

d7d285f9708c0e35970fa05965a3f54c

Ministry of Health Medical Device Import No. 027140

DHA05602714003

Company Information

France

Product Details

I General and plastic surgical devices

I3300 Surgical mesh

Imported from abroad

Dates and Status

Mar 19, 2015

Mar 19, 2025

Sep 05, 2022

Cancellation Information

Logged out

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